Recovery process for functionalized compound reaction product

Abstract

Provided is a process for recovery of a functionalized compound reaction product comprising contacting (i) an oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond, in an acidic medium to form a reaction milieu comprising a functionalized compound reaction product, contacting the reaction milieu with a water-immiscible organic solvent, separating the water-immiscible organic solvent from the reaction milieu, wherein the functionalized compound reaction product is dissolved in the water-immiscible organic solvent, and separating the functionalized compound reaction product and the water-immiscible organic solvent. The water-immiscible extraction solvent can be the same compound as the compound comprising as least one CH bond, for example, propane or n-butane.

Claims

1. A process for recovery of a functionalized compound reaction product that is soluble in a water-immiscible organic solvent comprising contacting (i) an oxidizing electrophile comprising a main group element selected from the group consisting of thallium, lead, bismuth, antimony, selenium, arsenic, tellurium, and a mixture thereof, and (ii) a compound comprising at least one CH bond that is an alkane, a heteroalkane, or an arene, in an aqueous acidic medium to form a reaction milieu comprising a reaction product that is an alkane oxygenate, heteroalkane oxygenate, or arene oxygenate, respectively, wherein at least one CH bond of the starting alkane, heteroalkane, or arene compound comprising at least one CH bond is replaced with an oxygenate group, and wherein the reaction product is soluble in a water-immiscible organic solvent, contacting the reaction milieu with a water-immiscible organic solvent that is a hydrocarbon solvent in which the reaction product is soluble, separating the water-immiscible organic solvent from the reaction milieu, wherein the reaction product is dissolved in the water-immiscible organic solvent, and separating the reaction product and the water-immiscible organic solvent.

2. The process of claim 1, wherein the compound comprising at least one CH bond is an alkane.

3. The process of claim 2, wherein the alkane is selected from the group consisting of methane, ethane, propane, butane, and a mixture thereof.

4. The process of claim 1, wherein the compound comprising at least one CH bond is a heteroalkane that is an alcohol.

5. The process of claim 1, wherein the compound comprising at least one CH bond is an arene that is an aryl ring system or a heteroaryl ring system.

6. The process of claim 1, wherein the aqueous acidic medium comprises an aqueous carboxylic acid.

7. The process of claim 1, wherein the reaction product is an ester or a diester.

8. The process of claim 7, wherein the compound comprising at least one CH bond is propane and the reaction product is 1,2-propanediol diacetate.

9. The process of claim 1, wherein the hydrocarbon solvent is a straight chain, branched chain, or cyclic hydrocarbon, or a mixture thereof.

10. The process of claim 9, wherein the hydrocarbon solvent is a straight chain hydrocarbon comprising 2 to about 20 carbon atoms.

11. The process of claim 10, wherein the straight chain hydrocarbon is propane, n-butane, or n-pentane.

12. The process of claim 9, wherein the hydrocarbon solvent is a branched chain hydrocarbon comprising 4 to about 20 carbon atoms.

13. The process of claim 12, wherein the branched chain hydrocarbon is isobutane, isopentane, or tert-pentane.

14. The process of claim 1, wherein the water-immiscible organic solvent used for separating the reaction product is the same as the compound comprising as least one CH bond.

15. The process of claim 14, wherein the compound comprising at least one CH bond and the water-immiscible organic solvent are both propane or n-butane.

16. The process of claim 1, wherein the reaction product and the water-immiscible organic solvent are separated by distillation.

17. The process of claim 1, wherein the reaction product has a higher boiling point than the aqueous acidic medium.

18. The process of claim 1, wherein (i) contacting the oxidizing electrophile comprising a main group element and the compound comprising at least one CH bond in the aqueous acidic medium, (ii) contacting the reaction milieu with the water-immiscible organic solvent, and (iii) separating the water-immiscible organic solvent from the reaction milieu are all carried out as a continuous process.

19. The process of claim 1, wherein the oxidizing electrophile comprises a main group element selected from the group consisting of lead, bismuth, antimony, selenium, arsenic, tellurium, and a mixture thereof.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) The invention related to a process for recovery of a functionalized compound reaction product comprising

(2) contacting (i) an oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond, in an acidic medium to form a reaction milieu comprising a functionalized compound reaction product,

(3) contacting the reaction milieu with a water-immiscible organic solvent,

(4) separating the water-immiscible organic solvent from the reaction milieu, wherein the functionalized compound reaction product is dissolved in the water-immiscible organic solvent, and

(5) separating the functionalized compound reaction product and the water-immiscible organic solvent.

(6) In the process, the compound comprising at least one CH bond, i.e., the compound to be functionalized, is an alkane, a heteroalkane, or an arene, as described herein.

(7) An alkane is a compound that includes at least one sp.sup.3-hybridized carbon atom, in which at least one substituent of that carbon atom is a hydrogen atom such that a CH bond is present. The alkane can be a straight-chain or branched alkane containing from, for example, from about 1 to about 16 carbon atoms (e.g., from about 1 to about 12 carbon atoms, from about 1 to about 10 carbon atoms, from about 1 to about 8 carbon atoms, from about 1 to about 6 carbon atoms, or from about 1 to about 4 carbon atoms). Examples of alkyl group include methane, ethane, n-propane, isopropane, n-butane, sec-butane, isobutane, tert-butane, n-pentane, isopentane, n-hexane, and the like.

(8) A heteroalkane is a compound that includes at least one sp.sup.3-hybridized carbon atom, in which at least one substituent of that carbon atom is a hydrogen atom such that a CH bond is present. The alkane portion of the heteroalkane implies a straight-chain or branched alkyl substituent containing from, for example, from about 1 to about 16 carbon atoms (e.g., from about 1 to about 12 carbon atoms, from about 1 to about 10 carbon atoms, from about 1 to about 8 carbon atoms, from about 1 to about 6 carbon atoms, or from about 1 to about 4 carbon atoms). The heteroalkane additionally comprises at least one heteroatom, i.e., an atom that is not a carbon or a hydrogen. Examples of heteroatoms include atoms of elements such as oxygen, sulfur, nitrogen, a halogen (e.g., chlorine), and/or a metal (e.g., tin). Thus, a heteroalkane substrate as the term is used herein can be, for example, an alkylcarbinol, an alkylamine, an alkylthiol, a halocarbon, or an organometallic compound. Examples of heteroalkane substrates useful for practice of a method of the invention include alcohols (e.g., n-propanol or n-butanol) and compounds comprising an ether oxygen, an ester, or an amide group. For instance, a method of the invention can be used to provide reaction products of heteroalkanes such as butanol, halobutanes, and butanoyl compounds, such as esters and amides.

(9) An arene, as the term is used herein, refers to an organic compound comprising at least one sp.sup.2-hybridized carbon atom bearing a hydrogen atom, in which the arene compound can further comprise (i) one or more sp.sup.3-hybridized carbon atoms, (ii) one or more heteroatoms, or (iii) both (i) and (ii). The term arene encompasses aryl and heteroaryl ring systems.

(10) The term aryl refers to an unsubstituted or substituted aromatic carbocyclic moiety, as commonly understood in the art, and includes monocyclic and polycyclic aromatics such as, for example, benzene, biphenyl, naphthalene, anthracene, pyrene, and the like. An aryl moiety generally contains from, for example, 6 to 30 carbon atoms, from 6 to 18 carbon atoms, from 6 to 14 carbon atoms, or from 6 to 10 carbon atoms. It is understood that the term aryl includes carbocyclic moieties that are planar and comprise 4n+2 electrons, according to Hckel's Rule, wherein n=1, 2, or 3. The aryl can be substituted or unsubstituted, as described herein.

(11) The term heteroaryl refers to aromatic 5 or 6 membered monocyclic groups, 9 or 10 membered bicyclic groups, and 11 to 14 membered tricyclic groups which have at least one heteroatom (O, S, or N) in at least one of the rings. Each ring of the heteroaryl group containing a heteroatom can contain one or two oxygen or sulfur atoms and/or from one to four nitrogen atoms provided that the total number of heteroatoms in each ring is four or less and each ring has at least one carbon atom. The fused rings completing the bicyclic and tricyclic groups can contain only carbon atoms and can be saturated, partially saturated, or unsaturated. The nitrogen and sulfur atoms can optionally be oxidized, and the nitrogen atoms can optionally be quaternized. Heteroaryl groups which are bicyclic or tricyclic must include at least one fully aromatic ring but the other fused ring or rings can be aromatic or non-aromatic. The heteroaryl group can be attached at any available nitrogen or carbon atom of any ring. Illustrative examples of heteroaryl groups are quinoline, pyridine, pyridazine, pyrimidine, pyrazine, benzimidazole, triazine, imidazole, (1,2,3)- and (1,2,4)-triazole, pyrazine, tetrazole, furan, pyrrole, thiophene, isothiazole, thiazole, isoxazole, and oxadiazole. The heteroaryl can be substituted or unsubstituted, as described herein.

(12) Examples of suitable arene substrates include aryls, such as benzene, phenols, phenolic ethers, derivatives of anilines, haloaryl compounds, naphthalene, and the like. Further examples of suitable arene substrates include heteroaryls, such as pyridine, quinoline, pyrrole, indole, thiophene, and the like. In an embodiment, the arene is benzene, pyridine, quinoline, or naphthalene, each of which is optionally substituted.

(13) A substituted arene typically comprises at least one substituent (e.g., 1, 2, 3, 4, 5, 6, etc.) in any suitable position (e.g., 1-, 2-, 3-, 4-, 5-, or 6-position, etc.). Suitable substituents include, e.g., halo, alkyl, alkenyl, alkynyl, hydroxy, nitro, cyano, amino, alkylamino, alkoxy, aryloxy, aralkoxy, carboxyl, carboxyalkyl, carboxyalkyloxy, amido, alkylamido, haloalkylamido, aryl, heteroaryl, and heterocycloalkyl. In an embodiment, the arene can be substituted with one or more heteroatoms and/or one or more alkyl groups. Examples of heteroatoms include atoms of elements such as oxygen, nitrogen, sulfur, a halogen (e.g., chlorine), and/or a metal (e.g., tin), e.g., aryl or heteroaryl alcohols (phenols), thiols, alkoxys, esters, halocarbons, carboxylic acids, and carboxamides.

(14) In some embodiments, the compound comprising at least one CH bond is an alkane. Preferably the alkane is methane, ethane, propane, butane, or a mixture thereof. Preferably the alkane is propane or butane. In other embodiments, the compound comprising at least one CH bond is a heteroalkane. Preferably the heteroalkane is an alcohol. In a particular embodiment, the compound is n-butanol or n-propanol. In still other embodiments, the compound comprising at least one CH bond is an arene, such as an aryl ring system (e.g., benzene or toluene) or a heteroaryl ring system.

(15) In an embodiment of the process, the functionalized compound reaction product is an oxidation reaction product, such as, for example, an ester or a diester. For example, when the starting compound with at least one CH bond is propane, a suitable oxidation reaction product is 1,2-propanediol diacetate.

(16) The oxidizing electrophile of any of the methods described herein comprises a main group element. A main group element, as the term is used herein, refers to metals and non-metals, including elements of CAS groups IIIA, IVA, VA, VIA, and VIIA, that are post-transition elements, i.e., being of higher atomic number than the last element of the first transition series, Zn, i.e., of atomic number >30. In an embodiment, the main group element is an element selected from CAS groups IIIA, IVA, VA, and VIA. Thus, an oxidizing electrophile used in practice of methods of the invention includes elements having stable isotopic forms of atomic numbers 31-35, 49-53, and 81-83. In a preferred embodiment, the oxidizing electrophile includes at least one element that is a stable isotopic form of any one of atomic numbers 31-34, 49-52, and 81-83. The main group element, in some embodiments, has a d.sup.10 electronic configuration. However, an oxidizing electrophile used in practice of a method of the invention can have other than a d.sup.10 electronic configuration. The main group element can cycle between a higher oxidation state (in the oxidizing electrophile reagent that reacts with the alkane CH bond) and a lower oxidation state (an electrophile reduction product, from which the oxidizing electrophile can be regenerated, either in situ or in a discrete step). By this means, an economically and environmentally favorable self-contained system for alkane, heteroalkane, or arene conversion, e.g., to alkane, heteroalkane, or arene oxygenates, respectively, can be formed, consuming only a second oxidant (e.g., a peroxide such as hydrogen peroxide, oxygen, ozone, nitric acid, or a halogen such as chlorine). In an embodiment, the main group element in oxidized form is in an oxidation state of +n. In other embodiments, the main group element is in an oxidation state of +(n2) or +(n1) for an electrophile reduction product that is formed by the oxidizing electrophile.

(17) As known in the art, an oxidizing electrophile can be known as a soft oxidizing electrophile. A soft electrophile, as the term is used herein, relates to classification under the hard/soft acid/base (HSAB) concept, known as the Pearson acid base concept, which assigns the terms hard or soft and the terms acid or base to chemical species. The term hard applies to species that are weakly polarizable, whereas the term soft applies to species that are strongly polarizable. See R. G. Pearson, Chemical HardnessApplications From Molecules to Solids, Wiley-VCH, Weinheim, 1997.

(18) Table 1 is a listing of exemplary species based on Pearson hard and soft theory. Oxidizing electrophiles used in practice of methods of the invention are classified as soft according to the HSAB theory, and include forms of main group elements such as Tl, Pb, Bi, Sb, Se, Te, and I. Higher oxidation states of these elements, as salts or compounds thereof, are used as the soft oxidizing electrophiles for practice of methods of the invention.

(19) TABLE-US-00001 TABLE 1 Classification of Pearson Hard and Soft Acids Hard Acids Borderline Acids Soft Acids H.sup.+, Li.sup.+, Na.sup.+, K.sup.+, Be.sup.+2, Mg.sup.+2, Fe.sup.+2, Co.sup.+2, Ni.sup.+2, Zn.sup.+2, Rh.sup.+3, Pd.sup.+2, Pt.sup.+2, Pt.sup.+4, Cu.sup.+, Ag.sup.+, Ca.sup.+2, Ba.sup.+2, Sc.sup.+3, La.sup.+2, Ce.sup.+4, Ir.sup.+3, Ru.sup.+3, Os.sup.+3, B(CH.sub.3).sub.3, Au.sup.+, Cd.sup.+2, Hg.sup.+, Hg.sup.+2, Tl.sup.+3, Gd.sup.+3, Lu.sup.+3, Th.sup.+4, U.sup.+4, UO.sub.2.sup.+2, GaH.sub.3, R.sub.3C+, C.sub.4H.sub.5+, Sn.sup.+2, Ph.sup.+4, Bi.sup.+5, Br.sup.+, Br.sub.2, I.sup.+, I.sub.2, Ti.sup.+4, Zr.sup.+4, Hf.sup.+4, VO.sup.+2, Cr.sup.+3, Pb.sup.+2, NO.sup.+, Sb.sup.+3, Bi.sup.+3, SO.sub.2 Se.sup.+6, Te.sup.+6, I.sup.+3 BF.sub.3, BCl.sub.3, Al.sup.+3, AlCl.sub.3, CO.sub.2, RCO.sup.+, NC.sup.+, Si.sup.+4, Sn.sup.+4

(20) Other soft acids are known to those of skill in the art, and elements having suitable pairs of oxidation states can be selected by the person of skill in the art for practicing the methods of the invention.

(21) In some embodiments, the oxidizing electrophile comprises a main group element selected from thallium, lead, bismuth, antimony, selenium, tellurium, iodine, and a mixture thereof, each of which is in oxidized form. In a particular embodiment, the oxidizing electrophile comprises a main group element selected from thallium, lead, bismuth, antimony, selenium, tellurium, and a mixture thereof, each of which is in oxidized form. In the case of Hg, Tl, and Pb, the oxidized forms that are most active are those that have the electronic configuration of Xe, 5d.sup.10, 6s.sup.0. However, this need not be the electronic configuration of systems that react since I(III), with an electronic configuration of Kr, 4d.sup.10, 5s.sup.2, 5p.sup.2, is found to be active for CH activation. In particular embodiments, the oxidizing electrophile can comprise thallium(III), lead(IV), bismuth(V), iodine(III), Sb(V), iodine(V), or a mixture of any of the foregoing elements. In a preferred embodiment, the oxidizing electrophile comprises thallium(III), lead(IV), bismuth(V), Sb(V), or any mixture thereof. In an embodiment, the oxidizing electrophile comprises thallium(III). In another embodiment, the oxidizing electrophile comprises lead(IV). In yet another embodiment, the oxidizing electrophile comprises bismuth(V). In still yet another embodiment, the oxidizing electrophile comprises Sb(V).

(22) In some embodiments, the oxidizing electrophile comprising a main group element in oxidized form is a salt, wherein the counterion of the main group element in oxidized form is a conjugate anion of an acid (e.g., one or more trifluoroacetate, acetate, sulfate, and/or alkylsulfonate anions). For example, the oxidizing electrophile can have the formula M.sup.+nX.sub.n, in which M is a metal or non-metal main group element cation in an oxidation state of n, X is an anionic counterion, and n is the number of anionic charges necessary to balance the n+ positive charge of the metal ion. The anionic counterion (X) is any suitable anionic counterion/ligand, including one or more trifluoroacetate, acetate, sulfate, and/or alkylsulfonate anions.

(23) In an embodiment of any of the processes described herein, the reaction of (i) the oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond is carried out in an acidic medium, including an aqueous acidic medium. The acidic acid is any suitable acid, such as a mineral acid, a carboxylic acid, a sulfonic acid, aqueous solutions thereof, or any combination thereof. In some embodiments, the acidic medium comprises an aqueous carboxylic acid (e.g., formic acid, acetic acid, butyric acid, caproic acid, trifluoracetic acid). Preferably the carboxylic acid is acetic acid or trifluoracetic acid.

(24) The acidic medium further comprises a water-immiscible organic solvent. The water-immiscible organic solvent is any suitable solvent that undergoes phase separation from an aqueous media under processing conditions (e.g., at room temperature or at an elevated temperature, such as greater than 30 C., greater than 40 C., greater than 50 C., greater than 60 C., greater than 70 C., greater than 80 C., greater than 90 C., or greater than 100 C.) such that the water-immiscible organic solvent acts as an extraction solvent. In some embodiments, the water-immiscible organic solvent comprises a hydrocarbon solvent, an oxycarbon solvent, or a mixture thereof. In other embodiments, the extraction solvent comprises a mixture of two or more solvents, such as a mixture of straight chain hydrocarbons, branched chain hydrocarbons, cycloalkyl hydrocarbons, aryl hydrocarbons, arylalkyl hydrocarbons, and/or oxycarbons.

(25) The hydrocarbon solvent comprises a straight chain, branched chain, or cyclic hydrocarbon, or a mixture thereof. In some embodiments, the hydrocarbon solvent comprises a straight chain hydrocarbon comprising 2 to about 20 carbon atoms (e.g., 2 carbon atoms, 3 carbon atoms, 4 carbon atoms, 5 carbon atoms, 6 carbon atoms, 7 carbon atoms, 8 carbon atoms, 9 carbon atoms, 10 carbon atoms, 11 carbon atoms, 12 carbon atoms, 13 carbon atoms, 14 carbon atoms, 15 carbon atoms, 16 carbon atoms, 17 carbon atoms, 18 carbon atoms, 19 carbon atoms, or 20 carbon atoms or any range thereof). For example, the hydrocarbon solvent can be propane, butane, pentane, hexane, heptane, dodecane, octadecene, or ligroin, or a mixture thereof. Preferably the straight chain hydrocarbon is propane, n-butane, or n-pentane, or a mixture thereof. In some embodiments, the hydrocarbon solvent is a branched chain hydrocarbon comprising 4 to about 20 carbon atoms (e.g., 4 carbon atoms, 5 carbon atoms, 6 carbon atoms, 7 carbon atoms, 8 carbon atoms, 9 carbon atoms, 10 carbon atoms, 11 carbon atoms, 12 carbon atoms, 13 carbon atoms, 14 carbon atoms, 15 carbon atoms, 16 carbon atoms, 17 carbon atoms, 18 carbon atoms, 19 carbon atoms, or 20 carbon atoms or any range thereof). Preferably the branched chain hydrocarbon is isobutane, isopentane, or tert-pentane, or a mixture thereof. In some embodiments, the hydrocarbon solvent comprises a cyclic hydrocarbon comprising between 3 and about 20 carbon atoms (e.g., 3 carbon atoms, 4 carbon atoms, 5 carbon atoms, 6 carbon atoms, 7 carbon atoms, 8 carbon atoms, 9 carbon atoms, 10 carbon atoms, 11 carbon atoms, 12 carbon atoms, 13 carbon atoms, 14 carbon atoms, 15 carbon atoms, 16 carbon atoms, 17 carbon atoms, 18 carbon atoms, 19 carbon atoms, or 20 carbon atoms or any range thereof). Examples of a cyclic hydrocarbon include cyclopentane, cyclohexane, cyclohexene, methylcyclohexane, cycloheptane, and cyclooctane. In other embodiments, the extraction solvent comprises an aryl or arylalkyl hydrocarbon, containing between 6 and about 20 carbon atoms (e.g., 6 carbon atoms, 7 carbon atoms, 8 carbon atoms, 9 carbon atoms, 10 carbon atoms, 11 carbon atoms, 12 carbon atoms, 13 carbon atoms, 14 carbon atoms, 15 carbon atoms, 16 carbon atoms, 17 carbon atoms, 18 carbon atoms, 19 carbon atoms, or 20 carbon atoms or any range thereof). Examples of an aryl or arylalkyl hydrocarbon include benzene, toluene, xylenes, pentamethylbenzene, tetramethylbenzene (durene), limonene, and the like.

(26) An oxycarbon solvent is any hydrocarbon comprising one or more oxygen atoms, such as an ether, an ester, a ketone, or a carboxylic acid comprising between 4 and about 20 carbon atoms (e.g., 4 carbon atoms, 5 carbon atoms, 6 carbon atoms, 7 carbon atoms, 8 carbon atoms, 9 carbon atoms, 10 carbon atoms, 11 carbon atoms, 12 carbon atoms, 13 carbon atoms, 14 carbon atoms, 15 carbon atoms, 16 carbon atoms, 17 carbon atoms, 18 carbon atoms, 19 carbon atoms, or 20 carbon atoms or any range thereof). Examples of an oxycarbon solvent include diethyl ether, diisopropyl ether, di-t-butyl ether, methyl t-butyl ether, ethyl t-butyl ether, methoxyethane, dimethoxyethane, dimethoxymethane, 1,4-dioxane, morpholine, diethylene glycol diethyl ether, diglyme, tetrahydrofuran, tetrahydropyran, ethyl acetate, methyl acetate, methoxypropyl acetate, n-butyl acetate, methanol, ethanol, n-propanol, i-propanol, 1,3-propanediol, n-butanol, 2-butanol, i-butanol, t-butyl alcohol, 1,4-butanediol, 1,2,4-butanetriol, 2-methyl-1butanol, 3-methyl-2-butanol, 2-methyl-1-pentanol, 2-pentanol, neopentyl alcohol, tert-amyl alcohol, 2-ethylhexanol, glycerol, ethylene glycol, diethylene glycol, propylene glycol, benzyl alcohol, and the like.

(27) The result of the separation step using the water-immiscible organic solvent is an aqueous acidic medium containing main group metal salts, i.e., the electrophile reduction product depleted in oxygenation product, and an extraction solvent solution containing the desired oxidation product.

(28) The oxidation product that is extracted from the reaction mixture by use of the water-immiscible organic solvent (e.g., a hydrocarbon and/or oxycarbon solvent) can be recovered from the extraction solution by distillation, such as simple distillation or fractional distillation, or by other suitable separation methods (e.g., decantation, evaporation, or chromatography). The oxidation product of the reaction can have a lower or a higher boiling point than the water-immiscible organic solvent. In an embodiment, the functionalized compound reaction product has a higher boiling point than the acidic medium.

(29) The aqueous phase of the reaction milieu following solvent extraction of the reaction mixture can contain residual amounts of the immiscible organic solvent (extraction solvent) after phase separation. The residual immiscible organic solvent can be removed by further extraction with the reactant compound comprising at least one CH bond leading to an aqueous acidic medium substantially free from the extraction solvent. An aqueous acidic medium that is substantially free from the extraction solvent contains, for example, less than 20% by volume of the extraction solvent (e.g., less than 15% by volume, less than 10% by volume, less than 5% by volume, less than 2% by volume, or less than 1% by volume).

(30) In an embodiment of any of the processes described herein, the water-immiscible extraction solvent is the same as the compound comprising as least one CH bond. For example, the compound comprising at least one CH bond and the water-immiscible extraction solvent can both be propane or n-butane. For instance, propane in the reaction with the oxidizing electrophile in an aqueous carboxylic acid medium can yield a mixture of propanol and propanediol esters. More specifically, if the carboxylic acid medium comprises acetic acid, 1,2-propanediol diacetate can be the reaction product. This reaction product can be removed from the reaction milieu by extraction with liquid propane, i.e., under pressure. Next, the liquid propane extraction solvent and 1,2-propanediol diacetate can be separated by fractional distillation to provide the 1,2-propanediol diacetate substantially free of acetic acid and main group metal acetate salts.

(31) By the use of the extraction process as disclosed and claimed herein, a more economically advantageous method for recovery of the valuable functionalized compound reaction products, such as the esters exemplified above, can be achieved. There are advantages to use of the extraction process as disclosed herein relative to simple distillation of the solvent milieu that contains a desired product. For instance, the reaction products may be less volatile than the acidic reaction medium (e.g., carboxylic acid), in which case high energy costs would be incurred by the need to distill away the acid medium (e.g., carboxylic acid) before recovering the reaction product. By use of a method of the invention, a higher-boiling oxidation product from the reaction can be first separated from the acid medium (e.g., carboxylic acid), and from the electrophile reduction product (inorganic salts), prior to recovery from the extraction solvent, minimizing the need to distill the acid reaction solvent and avoiding potential overheating and formation of thermal by-products. Moreover, in an embodiment, all three steps, i.e., (i) contacting an oxidizing electrophile comprising a main group element and a compound comprising at least one CH bond in an acidic medium, preferably comprising an aqueous carboxylic acid, (ii) contacting the reaction milieu with a water-immiscible organic solvent, and (iii) separating the water-immiscible organic solvent can be carried out as a continuous process.

(32) The invention is further illustrated by the following embodiments.

(33) (1) A process for recovery of a functionalized compound reaction product comprising contacting (i) an oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond, in an acidic medium to form a reaction milieu comprising a functionalized compound reaction product, contacting the reaction milieu with a water-immiscible organic solvent, separating the water-immiscible organic solvent from the reaction milieu, wherein the functionalized compound reaction product is dissolved in the water-immiscible organic solvent, and separating the functionalized compound reaction product and the water-immiscible organic solvent.

(34) (2) The process of embodiment (1), wherein the compound comprising at least one CH bond is an alkane, a heteroalkane, or an arene, wherein the heteroalkane comprises at least one sp.sup.3-hybridized carbon atom bearing a hydrogen atom and at least one heteroatom other than a carbon or hydrogen atom, and the arene comprises at least one sp.sup.2-hybridized carbon atom bearing a hydrogen.

(35) (3) The process of embodiment (2), wherein the compound comprising at least one CH bond is an alkane, preferably methane, ethane, propane, butane, or a mixture thereof.

(36) (4) The process of embodiment (2), wherein the compound comprising at least one CH bond is a heteroalkane, preferably an alcohol.

(37) (5) The process of embodiment (2), wherein the compound comprising at least one CH bond is an arene, preferably an aryl ring system or a heteroaryl ring system.

(38) (6) The process of any one of embodiments (1)-(5), wherein the acidic medium comprises an aqueous carboxylic acid, preferably acetic acid or trifluoracetic acid

(39) (7) The process of any one of embodiments (1)-(6), wherein the functionalized compound reaction product is an oxidation reaction product.

(40) (8) The process of embodiment (7), wherein the oxidation reaction product is an ester or a diester.

(41) (9) The process of embodiment (8), wherein the hydrocarbon is propane and the hydrocarbon oxidation reaction product is 1,2-propanediol diacetate.

(42) (10) The process of any one of embodiments (1)-(9), wherein the water-immiscible organic solvent is a hydrocarbon solvent, an oxycarbon solvent, or a mixture thereof.

(43) (11) The process of embodiment (10), wherein the hydrocarbon solvent is a straight chain, branched chain, or cyclic hydrocarbon, or a mixture thereof.

(44) (12) The process of embodiment (11), wherein the straight chain hydrocarbon comprises 2 to about 20 carbon atoms.

(45) (13) The process of embodiment (12), wherein the straight chain hydrocarbon is propane, n-butane, or n-pentane.

(46) (14) The process of embodiment (11), wherein the branched chain hydrocarbon comprises 4 to about 20 carbon atoms.

(47) (15) The process of embodiment (14), wherein the branched chain hydrocarbon is isobutane, isopentane, or tert-pentane.

(48) (16) The process of any one of embodiments (1)-(15), wherein the water-immiscible extraction solvent is the same as the compound comprising as least one CH bond.

(49) (17) The process of embodiment (16), wherein the compound comprising at least one CH bond and the water-immiscible extraction solvent are both propane.

(50) (18) The process of embodiment (16), wherein the compound comprising at least one CH bond and the water-immiscible extraction solvent are both n-butane.

(51) (19) The process of any one of embodiments (1)-(18), wherein the functionalized compound reaction product and the water-immiscible organic solvent are separated by distillation.

(52) (20) The process of any one of embodiments (1)-(19), wherein the functionalized compound reaction product has a higher boiling point than the acidic medium.

(53) (21) The process of any one of embodiments (1)-(20), wherein (i) contacting an oxidizing electrophile comprising a main group element and a compound comprising at least one CH bond in an acidic medium, preferably comprising an aqueous carboxylic acid, (ii) contacting the reaction milieu with a water-immiscible organic solvent, and (iii) separating the water-immiscible organic solvent are all carried out as a continuous process.

(54) All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.

(55) The use of the terms a and an and the and at least one and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The use of the term at least one followed by a list of one or more items (for example, at least one of A and B) is to be construed to mean one item selected from the listed items (A or B) or any combination of two or more of the listed items (A and B), unless otherwise indicated herein or clearly contradicted by context. The terms comprising, having, including, and containing are to be construed as open-ended terms (i.e., meaning including, but not limited to,) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., such as) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.

(56) Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.