Process for preparing electron deficient olefin precursors

Abstract

This invention relates to a process for producing electron deficient olefin precursors, such as 2-cyanoacetates, using an acid catalyzed esterification reaction.

Claims

1. A process for the preparation of a cyanoacetate, steps of which comprise: (a) reacting cyanoacetic acid and an alcohol, in the presence of a catalyst comprising a lanthanide element or a transition element, under appropriate conditions and for a time sufficient to yield a cyanoacetate; (b) optionally, separating therefrom the so formed cyanoacetate substantially free from the cyanoacetic acid, the alcohol, and/or catalyst, and by-products.

2. A process for the preparation of an electron deficient olefin precursor, steps of which comprise: (a) reacting: (i) a 2-electron withdrawing group-substituted methylene compound embraced by: ##STR00006## wherein EWG represents an electron withdrawing group selected from the group consisting of cyano or nitrile, alkoxy or aryloxy, carboxyl, sulphonic acids, carbonyls, halogens, nitro, isocyanate, sulfoxide and phosphine oxide; and R here represents hydrogen; and (ii) an alcohol, in the presence of a catalyst comprising a lanthanide element or a transition element, under appropriate conditions and for a time sufficient to yield an electron deficient olefin precursor embraced by: ##STR00007## wherein EWG represents an electron withdrawing group selected from the group consisting of cyano or nitrile, alkoxy or aryloxy, carboxyl, sulphonic acids, carbonyls, halogens, nitro, isocyanate, sulfoxide and phosphine oxide; and R here represents straight chain, branched, cyclic or fused C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, and C.sub.6-20 aryl or C.sub.7-20 alkaryl, with or without substitution or interruption by one or more heteroatoms; and (c) optionally, separating therefrom the so formed electron deficient olefin precursor substantially free from the cyanoacetic acid, the alcohol, and/or catalyst, and by-products.

3. The process of claim 1, wherein the catalyst comprising a lanthanide element or a transition element has one or more ligands bound to the element(s).

4. The process of claim 1, wherein the catalyst comprises a lanthanide element.

5. The process of claim 1, wherein the catalyst comprises a transition element.

6. The process of claim 1, wherein the catalyst comprises ytterbium.

7. The process of claim 1, wherein the catalyst comprises niobium, zirconium or scandium.

8. The process of claim 3, wherein the one or more ligands is selected from halogens, triflates, mesylates, nitrates or tosylates.

9. The process of claim 1, wherein the alcohol is any mono-, di- or multi-functional hydroxyl compound.

10. The process of claim 1, wherein the alcohol is any mono-, di- or multi-functional C.sub.1-20 alkanol, C.sub.2-20 alkenol, or C.sub.2-20 alkynol.

11. The process of claim 1, wherein the alcohol is an aromatic alcohol.

12. The process of claim 1, wherein the alcohol is phenol or benzyl alcohol.

13. The process of claim 2, wherein the so-formed electron deficient olefin precursor is a cyanoacetate.

14. A process for the preparation of a cyanoacetate, steps of which comprise: (a) reacting cyanoacetic acid and an alcohol, in the presence of a catalyst comprising a lanthanide element or a transition element, under appropriate conditions and for a time sufficient to yield a cyanoacetate; (b) optionally, separating the so formed cyanoacetate substantially free from the cyanoacetic acid, the alcohol, and/or catalyst, and by-products.

15. The process of claim 2, wherein the catalyst comprising a lanthanide element or a transition element has one or more ligands bound to the element(s).

16. The process of claim 2, wherein the catalyst comprises a lanthanide element.

17. The process of claim 2, wherein the catalyst comprises a transition element.

18. The process of claim 2, wherein the catalyst comprises ytterbium.

19. The process of claim 2, wherein the catalyst comprises niobium, zirconium or scandium.

20. The process of claim 2, wherein the alcohol is any mono-, di- or multi-functional hydroxyl compound.

21. The process of claim 2, wherein the alcohol is any mono-, di- or multi-functional C.sub.1-20 alkanol, C.sub.2-20 alkenol, or C.sub.2-20 alkynol.

22. The process of claim 2, wherein the alcohol is an aromatic alcohol.

23. The process of claim 2, wherein the alcohol is phenol or benzyl alcohol.

Description

BRIEF DESCRIPTION OF THE FIGURE

(1) FIG. 1 depicts a synthetic scheme according to the present invention. More specifically, FIG. 1 shows the reaction of a cyanoacetic acid with an alcohol at ambient temperature in the presence of ytterbium trifluoromethane sulfonate [Yb(OTf).sub.3]. The reaction generates the target 2-cyanoacetate. In the FIGURE, R in the alcohol and the cyanoacetate represents straight chain, branched, cyclic or fused C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, and C.sub.6-20 aryl or C.sub.7-20 alkaryl, with or without substitution or interruption by one or more heteroatoms.

DETAILED DESCRIPTION

(2) As noted above, the present invention provides a process for the preparation of a reactive electron deficient olefin precursor. The process for the preparation of a reactive electron deficient olefin precursor is provided herein. In one, more focused, aspect, the invention includes the steps of:

(3) (a) reacting cyanoacetic acid and an alcohol, in the presence of a catalyst comprising a lanthanide element or a transition element, under appropriate conditions and for a time sufficient to yield a cyanoacetate;

(4) (b) optionally, separating so formed cyanoacetate substantially free from the cyanoacetic acid, the alcohol, and/or catalyst, and by-products.

(5) In another, more broad, aspect, the invention provides a process for the preparation of a reactive electron deficient olefin precursor that includes the steps of:

(6) (a) reacting: (i) a 2-electron withdrawing group-substituted methylene compound embraced by:

(7) ##STR00003##
where EWG represents an electron withdrawing group; and R here represents hydrogen; and (ii) an alcohol, in the presence of a catalyst comprising a lanthanide element or a transition element, under appropriate conditions and for a time sufficient to yield an electron deficient olefin precursor embraced by:

(8) ##STR00004##
where EWG represents an electron withdrawing group; and R here represents straight chain, branched, cyclic or fused C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, and C.sub.6-20 aryl or C.sub.7-20 alkaryl, with or without substitution or interruption by one or more heteroatoms;

(9) (b) optionally, separating so formed electron deficient olefin precursor substantially free from the 2-electron withdrawing group-substituted methylene compound, the alcohol, and/or the catalyst, and by-products.

(10) By the processes of the present invention yields of electron deficient olefin precursors may be greater than 70%, desirably 80% and more desirably 90%.

(11) In the more broad aspect noted above, the electron deficient olefin precursor so formed is embraced by:

(12) ##STR00005##
where EWG represents an electron withdrawing group, such as cyano or nitrile, alkoxy or aryloxy (which may itself be substituted by an EWG in the ortho and/or para position on the aromatic ring), carboxyl (e.g., carboxylic acids or carboxylic esters), sulphonic acids, carbonyls, halogens (e.g., F, Cl, Br, and I), nitro, isocyanate, sulfoxide and phosphine oxide; and R here represents straight chain, branched, cyclic or fused C.sub.1-20 alkyl or alkylenyl, C.sub.2-20 alkenyl or alkenylenyl, C.sub.2-20 alkynyl or alkynylenyl, and C.sub.6-20 aryl or arylenyl, or C.sub.7-20 alkaryl or alkarylenyl, with or without substitution or interruption by one or more heteroatoms.

(13) Reference to FIG. 1 may be useful to appreciate further the present invention, which is described in more detail below and in the Examples section that follows.

(14) As an initial reactant in the inventive processes is the so-described 2-electron withdrawing group-substituted carboxylic acid. Representative examples of the 2-electron withdrawing group-substituted carboxylic acid used as a reactant include malonic acid, glycolic acid, an alkyl (e.g., ethyl) nitroacetic acid, an alkyl (e.g., ethyl) haloacetic (like bromoacetic, chloroacetic, and iodoacetic), and cyanoacetic acid, some of which are commercially available for instance from Aldrich Chemical Co. A particularly desirable example of the 2-electron withdrawing group-substituted carboxylic acid is cyanoacetic acid.

(15) The amount of the 2-electron withdrawing group-substituted carboxylic acid that should be used in the inventive process is in the range of about 0.5 to about 2 equivalents, such as about 0.8 equivalents.

(16) Together with the 2-electron withdrawing group-substituted carboxylic acid as an initial reactant in the inventive processes is an alcohol.

(17) The alcohol may be any mono-, di- or multi-functional hydroxyl compound. Mono-, di- or multi-functional C.sub.1-20 alkanols, C.sub.2-20 alkenols, and C.sub.2-20 alkynols, whether straight chain, branched, cyclic or fused, may be used. Aromatic alcohols, such as phenol, benzyl alcohol and derivatives thereof, may be used.

(18) The alcohol should be used in an amount of about 0.5 to about 2 equivalents, such as about 0.8 equivalents.

(19) The alcohol and the compound should be used in a molar ratio of about 0.5 to about 2 equivalents, such as about 0.8 equivalents.

(20) As noted, the catalyst is one that comprises lanthanide element or a transition element. The catalyst is acidic in nature, as measured or determined by its ability to donate a hydrogen (proton or hydrogen ion, H.sup.+), or, alternatively, its ability to form a covalent bond with an electron pair.

(21) To the lanthanide element or the transition element is bonded, coordinated or complexed, as appropriate, one or more ligands. The ligands may be selected for instance from conventional leaving groups used in organic synthetic schemes. Halogens, tosylates, mesylates, nitrates and triflates are chief among ligands that are suitable for use herein.

(22) A prime example of a lanthanide element suitable for use in this connection is ytterbium, though others may also be useful, such as lanthanum, cerium, samarium, europium, and dysprosium. Prime examples of a transition element suitable for use in this connection is niobium, zirconium or scandium, with niobium being particularly desirable in this regard.

(23) Desirable catalysts for use in the inventive process include ytterbium trifluoromethane sulfonate [Yb(OTf).sub.3] and niobium halides, such as niobium chloride.

(24) The catalyst should be used in an amount of up to about 20 mol %, such as about 10 mol %.

(25) The electron deficient olefin precursor so formed by the inventive processes may be a variety of olefins having an electron withdrawing group attached to a carbon atom that is alpha to the carbonyl of a carboxylic acid ester.

(26) Representative examples of these electron deficient olefin precursors include esters of malonic acid, esters of glycolic acid, esters of nitroacetic acid (such as ethyl nitroacetate), esters of haloacetic acids (such as ethyl haloacetatelike bromoacetates, chloroacetates, and iodoacetates), esters of cyanoacetic acid (such as cyanoacetates), some of which are commercially available for instance from Aldrich Chemical Co.

(27) In a desirable embodiment, the reactive electron deficient olefin precursor so formed will be a 2-cyanoacetate.

(28) Representative examples of 2-cyanoacetates so formed by the inventive processes include those having ester groups of methyl, ethyl, propyl, isoamyl, propargyl, butyl, pentyl, hexyl, octyl, nonyl, oxononyl, decyl, dodecyl, allyl, ethynyl, butenyl, cyclohexyl, phenyl, phenethyl, tetrahydrofurfuryl, chloroethyl, 2,2,2-trifluoroethyl, hexafluoroisopropyl, methoxymethyl, methoxyethyl, thiomethoxyethyl, methoxybutyl, thiomethoxybutyl, ethoxyethyl, thioethoxyethyl, propoxyethyl, thioproxyethyl, butoxymethyl, thiobutoxymethyl, butoxyethyl, thiobutoxyethyl and dimethyl siloxane esters of 2-cyanoacetate. This recitation is by no means however exhaustive.

(29) While no solvent is ordinarily needed, the reaction of the inventive processes may proceed in solvent either forming a solution or a suspension. Solvents that may be used include acetonitrile, benzonitrile, chlorobenzene, nitromethane, tetrachloroethene, toluene, THF, 1,4-dioxane, and (poly)ethylene glycol dialkyl ethers or esters, and of course combinations thereof. Ionic liquids may also be used as a solvent. The reaction of the inventive processes may proceed with or without heating or cooling, depending of course on the specific reactants and the scale of the reaction.

(30) While the reaction ordinarily occurs at ambient temperature, gentle heating up to a temperature of 70 C. may be applied. The temperature may be reached through an external heating element or internally by means of the exotherm that may be generated depending on the identity of the reactants. The temperature of the reaction should be controlled however to accommodate any such exothermic processes.

(31) The time of reaction may be monitored by reference to the formation of the desired electron deficient olefin precursor product. .sup.1H NMR spectrometer is a particularly useful tool in this regard. The time of reaction may be as little as 30 minutes, for instance, or longer or shorter for that matter depending again on the identity of the specific reactants, the scale of the reaction and whether heat is added to the reaction conditions.

(32) Once formed, the electron deficient olefin precursor may be isolated as a product or may be used directly in situ to form an electron deficient olefin. The in situ use would be for instance as a reactant in a Knoevenagel condensation reaction with an aldehyde source conducted under conventional base catalyzed conditions or under state of the art acid catalyzed conditions.

(33) The following examples are intended to illustrate but in no way limit the present invention.

EXAMPLES

Example 1

(34) To a 50 ml round bottomed flask was added 4.76 g (0.056 mol) of cyanoacetic acid, 5.00 g (0.0675 mol) of n-butanol and 3.47 g (6.75 mmol, 10 mol %) of ytterbium triflate. The flask was fitted with a magnetic stirrer and rigorously stirred at a temperature of about 100 C. for a period of time of about 8.5 hours. The reaction was then taken up in 60 ml of deionised water and extracted three times with 20 ml portions of chloroform, dried over anhydrous MgSO.sub.4 and condensed under vacuum. The isolated yield of ethyl-2-cyanoacetate was 6.295 g, which is 79.50% with a purity determined by 500 MHz .sup.1H NMR of about 78-82%.

Example 2

(35) To a 25 ml round bottomed flask was added 9.527 g (0.112 mol) of cyanoacetic acid, 4.15 g (0.056 mol) of distilled n-butanol and 3.47 g (6.75 mmol, 10 mol %) of ytterbium triflate. The flask was fitted with a magnetic stirrer and rigorously stirred at room temperature for a period of time of 22 hours. The reaction was then taken up in 60 ml of deionised water and extracted three times with 20 ml portions of chloroform, dried over anhydrous MgSO.sub.4 and condensed under vacuum. The isolated yield of n-butyl-2-cyanoacetate was 5.692 g, which is 72.00% with a purity determined by 500 MHz .sup.1H NMR of about 94.5-97.5%.

Example 3

(36) To a 25 ml round bottomed flask was added 5.716 g (0.0672 mol) of cyanoacetic acid, 4.15 g (0.056 mol) of distilled n-butanol and 3.47 g (6.75 mmol, 10 mol %) of ytterbium triflate. The flask was fitted with a magnetic stirrer and rigorously stirred at room temperature for 24 hours. The reaction was then taken up in 60 ml of deionised water and extracted with three times with 20 ml portions of chloroform, dried over anhydrous MgSO.sub.4 and condensed under vacuum. The isolated yield of n-butyl cyanoacetate was 7.227 g, which is 91.50% with a purity determined by 500 MHz .sup.1H NMR to be about 92-93%.

Example 4

(37) To a 25 ml round bottomed flask was added 5.716 g (0.062 mol) of cyanoacetic acid, 4.936 g (0.056 mol) of 2-pentanol and 3.47 g (6.75 mmol, 10 mol %) of ytterbium triflate. The flask was fitted with a magnetic stirrer and rigorously stirred at room temperature for a period of time of 24 hours. The reaction was then taken up in 60 ml of deionised water and extracted three times with 20 ml portions of chloroform, dried over anhydrous MgSO4 and condensed under vacuum. The isolated yield of 2-pentyl cyanoacetate was 8.04 g, which is 92.57% with a purity determined by 500 MHz .sup.1H NMR of about 91-92%.

Example 5

(38) To a 25 ml round bottomed flask was added 7.15 g (0.084 mol) of cyanoacetic acid, 6.84 g (0.056 mol) of phenyl ethanol and 3.47 g (6.75 mmol, 10 mol %) of ytterbium triflate. The flask was fitted with a magnetic stirrer and rigorously stirred at room temperature for a period of time of 21 hours. The reaction was then taken up in 60 ml of deionised water and extracted three times with 20 ml portions of chloroform, dried over anhydrous MgSO4 and condensed under vacuum. The conversion to 2-phenyl ethyl cyanoacetate was determined by 500 MHz .sup.1H NMR to be 92.50-94.00% with a purity determined of about 94-94.50%.