LIGHT ASSISTED, CATALYST-FREE OXIDATION OF ALDEHYDES TO CARBOXYLIC ACIDS USING CARBON DIOXIDE

Abstract

Method for visible-light driven oxidation of aldehydes to carboxylic acid using carbon dioxide (CO.sub.2) as the oxidant in the absence of any catalyst are provided. In the disclosed process, aldehydes, when reacted with CO.sub.2 in an organic solvent, either in a batch reactor or in a continuous flow reactor, under conditions of ambient temperature and pressure, using a readily available household LED lamp, yield corresponding carboxylic acids along with the formation of carbon monoxide (CO) in the effluent gas.

Claims

1. A light assisted, catalyst-free photochemical process for oxidation of aldehydes using carbon dioxide, the process comprising: oxidizing an aldehyde with CO.sub.2 dissolved in a solvent under light irradiation in a batch or continuous flow photoreactor at a reaction temperature from 20° C. to 40° C. and a reaction pressure from 1 bar to 5 bar for an irradiation time from 1 hour to 24 hours to obtain a carboxylic acid product with formation of gaseous carbon monoxide as a co-product; and purifying the carboxylic acid product.

2. The process of claim 1, wherein the aldehyde is selected from: aromatic aldehydes substituted with an electron donating group or an electron deficient group; or aliphatic aldehydes.

3. The process of claim 1, wherein the aldehyde is an aryl aldehyde of Formula (I): ##STR00003## where R is selected from the group consisting of hydrogen, halogen, methyl, ethyl, propyl, butyl, amyl, isopropyl, isobutyl, phenyl, tolyl, biphenyl, benzyl, and naphthyl.

4. The process of claim 1, wherein the light irradiation comprises irradiating with a light source having a wavelength greater than 420 nm.

5. The process of claim 4, wherein the light source is a household LED light having a power from 10 W to 50 W.

6. The process of claim 1, wherein the solvent is selected from the group consisting of water, acetonitrile, dimethylformamide, dimethylsulfoxide, tetrahydrofuran, and mixtures thereof

7. The process of claim 6, wherein the solvent comprises acetonitrile.

8. The process of claim 1, wherein the irradiation time is from 1 hour to 15 hours.

9. The process of claim 1, wherein the reaction temperature is from 25° C. to 35° C. and a pressure of CO.sub.2 in the photoreactor is 1 atmosphere.

10. The process of claim 1, wherein the purifying comprises performing column chromatography on the carboxylic acid product in a silica gel bed.

11. The process of claim 1, wherein the process results in a yield of the carboxylic acid product from 30% to 97% determined on the basis of isolated carboxylic acid.

Description

BRIEF DESCRIPTION OF THE DRAWING

[0025] The FIGURE is a schematic of a reactor set-up for a continuous flow process.

DETAILED DESCRIPTION

[0026] Embodiments herein provide a catalyst-free process for the oxidation of aldehydes to carboxylic acids using CO.sub.2 as oxidant under mild reaction conditions.

[0027] Embodiments herein provide a method for the catalyst-free photochemical activation of CO.sub.2 to provide necessary oxygen for the oxidation along with the production of carbon monoxide as a by-product.

[0028] Embodiments herein provide a catalyst-free photochemical route for the preparation of carboxylic acids using CO.sub.2 as oxidant.

[0029] Embodiments herein provide to a catalyst-free photochemical route for the oxidation of aldehydes using CO.sub.2 as oxidant with the conversion from 30% to 99%.

[0030] Embodiments herein provide a catalyst-free photochemical route for the oxidation of aldehydes with CO.sub.2 at atmospheric pressure and ambient temperature ranges of 15° C. to 40° C., preferably at about 25° C.

[0031] Embodiments herein may include use of a polar solvent that is protic or aprotic or that is selected from water, acetonitrile or dimethylformamide or dimethylsulfoxide or tetrahydrofuran, or mixtures thereof as may be appropriate, in particular pure acetonitrile.

[0032] Embodiments herein provide a catalyst-free photochemical route for the oxidation of aldehydes to carboxylic acids in the time ranging from 1 hour to 24 hours.

[0033] Embodiments herein may include the use of a visible light source having wavelength (λ) greater than 420 nm or a broad spectrum of solar energy containing such wavelengths for the activation of the carbon dioxide under mild conditions.

[0034] Embodiments herein may include a catalyst-free photochemical route for the oxidation of aldehydes using CO.sub.2 as oxidant in a continuous flow reactor with the yield of the acid being from 20% to 80%.

[0035] Embodiments herein provide a catalyst-free photochemical reduction of CO.sub.2 to CO along with the simultaneous oxidation of aldehydes.

[0036] Specific embodiments of light assisted, catalyst-free photochemical process for oxidation of aldehydes using carbon dioxide will now be described. The processes may include reacting an aldehyde having a —CHO group in a polar organic solvent with carbon dioxide at temperature from 20° C. to 40° C. and at atmospheric pressure under the visible light irradiation to prepare the corresponding carboxylic acid along with the production of CO as a co-product in gaseous effluent.

[0037] As utilized herein including in the claims “oxidation of aldehyde” means insertion of an oxygen derived from the CO.sub.2 into the —CHO group of the compound to convert it into —COOH.

[0038] As utilized herein including in the claims “reactants” collectively references both aldehyde and CO.sub.2 (oxidant) and the “solvents” including both aqueous and organic reaction media.

[0039] Within this disclosure, “visible light” means light having a wavelength (λ) greater than 420 nm.

[0040] In embodiments, any compound having a —CHO group can be employed in the process described herein. Aromatic aldehydes—whether substituted by electron donating or electron deficient group—are preferred, but aliphatic aldehydes, either unsaturated and/or linear, can also be employed. Most of the aforementioned aldehydes are available commercially and may be used as received.

Constituents

[0041] Reactants

[0042] Embodiments herein relate to the oxidation of the aldehydes with CO.sub.2 without using any catalyst under light irradiation.

[0043] The aldehyde may be any organic compound containing a —CHO group. Aromatic aldehydes, which are suitable for the processes herein, include benzaldehyde and its substituted derivatives, heterocyclic aldehydes and analogously, the cyclic, or branched or chain isomers of aliphatic aldehydes, whether saturated or unsaturated, containing 4 to 10 carbon atoms, and their substituted variants.

[0044] Oxidant (Carbon Dioxide)

[0045] In embodiments herein, carbon dioxide is used as an oxidant in place of conventional oxidants such as O.sub.2 or H.sub.2O.sub.2 under visible illumination. In the reactions, of the two oxygen atoms present in carbon dioxide, one oxygen atom is converted in the oxidation of —CHO to —COOH and the other oxygen atom is converted to carbon monoxide. The reaction mixture containing substrates and solvent is either saturated with CO.sub.2 or is purged continuously with CO.sub.2 flow for effective oxidation.

[0046] Organic Solvents

[0047] Substrates (aldehyde and CO.sub.2) used in the embodiments herein are preferably dissolved in organic solvents. Polar organic solvents may be used owing to the higher solubility of CO.sub.2 in polar solvents. Suitable organic solvents include specifically, but not limited to, dimethylformamide (DMF), dimethylacetamide (DMA), acetonitrile (ACN), dimethylsulfoxide (DMSO), and N-methyl pyrolidone (NMP), or mixtures thereof.

Standard Protocol (Batch and Continuous Process)

[0048] According to embodiments, aldehyde substrate in a polar organic solvent, preferably acetonitrile (1:2 to 1:10 weight ratio with respect to the substrate) is taken into a 60-mL vessel for a batch process. The reaction mixture is saturated with CO.sub.2 by purging. The reaction vessel is sealed and irradiated with 20-W LED light for 1.0 hour to 15 hours. The intensity of the LED light at the reaction flask is measured to be 80 W/m.sup.2 to 100 W/m.sup.2 by an intensity meter. The progress of the reaction is monitored by thin layer chromatography using silica gel. After completion of the reaction, the solvent is evaporated under reduced pressure, and the concentrated residue is subjected to column chromatography on a silica gel (100-200 mesh) column using a 9:1 hexane-ethyl acetate solvent mixture as an eluent to afford pure carboxylic acid. The yield of the acid is obtained in a range of 30% to 98%. The formation of CO in the effluent gas is confirmed by Residual Gas Analysis (RGA).

[0049] In embodiments, a continuous process may be employed. A schematic experimental setup is provided in the FIGURE and includes a continuous-flow reactor assembly that includes a syringe pump, a digital mass flow controller, and non-return valves that are connected to a T-micro mixer for efficient mixing of reactant before sending to the reaction flow line. The continuous flow reactor line is 1000 mm long with an outer diameter of 3 mm and an inner diameter of 1.5 mm that is connected to a back-pressure regulator (BPR). The reactor is illuminated with visible light of intensity 80 W/m.sup.2 to 100 W/m.sup.2, and the product mixture is collected at the outlet of the rector.

[0050] While the processes herein are valuable for oxidizing aldehydes in general to obtain carboxylic acids, they are particularly useful for obtaining aromatic carboxylic acids from the corresponding aryl aldehydes such as benzaldehyde, tolualdehyde, anisaldehyde, chlorobenzaldehyde, and homologues thereof, as well as heterocyclic aldehydes such as furfural and analogues thereof.

[0051] Specific examples of suitable aldehydes used in the invention are aryl aldehydes corresponding to Formula (I):

##STR00002##

[0052] In Formula (I), R may be hydrogen, alkyl, aryl, chloro, or methoxy, for example. In specific examples, R of formula (I) may be hydrogen, halogen, methyl, ethyl, propyl, butyl, amyl, isopropyl, isobutyl, phenyl, tolyl, biphenyl, benzyl, or naphthyl, for example. Preferably, benzaldehyde and its substituted derivatives are utilized.

EXAMPLES

[0053] Following examples are given by way of illustration and therefore should not be construed to limit the scope of this disclosure or the appended claims.

Example 1

General Procedure for the Oxidation of Benzaldehyde

[0054] Benzaldehyde (1a) and polar organic solvent, preferably acetonitrile (1:2 to 1:10 weight ratio with respect to the substrate) was taken into a 60-mL vessel. The reaction mixture was saturated with CO.sub.2 by purging. The reaction vessel was sealed and irradiated with 20 W LED light for 2 h. The intensity of the LED light at the reaction flask was measured to be 86 W/m.sup.2 by intensity meter. The progress of the reaction was monitored by thin-layer chromatography using silica gel. After completion of the reaction, the solvent was evaporated under reduced pressure and the resulting concentrated residue was subjected to column chromatography on a silica gel (100-200 mesh) column using 9:1 hexane-ethyl acetate solvent mixture as eluent to afford pure benzoic acid as white crystals in 96% isolated yield.

Example 2

Oxidation of Benzaldehyde in Continuous Flow Reactor

[0055] Benzaldehyde (1a) was mixed with acetonitrile solvent in 1:2 to 1:5 weight ratio and pumped continuously through a syringe pump. The reactant solution was pumped at a flow rate of 72 μL/min and directed into the tubing of the reactor via T-micromixer. The CO.sub.2 was introduced into the system through MFC (mass flow controller) and was mixed with the solution in the T-micromixer to form a CO.sub.2-saturated reactant solution stream before sending it into a photochemical reactor. The combined flow rate was adjusted to the reactor volume of 7 mL with a residence time of 4 minutes at 20° C. A terminal BPR was connected with a 60 psi line to maintain the system pressure and prevent out-gassing. Benzoic acid product was obtained with 75% yield.

Example 3

Oxidation of Benzaldehyde in Dark

[0056] Benzaldehyde (1a) and polar organic solvent, preferably acetonitrile in (1:2 to 1:10 weight ratio with respect to the substrate) was taken into a 60-mL vessel. The reaction mixture was saturated with CO.sub.2 by purging. The reaction vessel was sealed and kept in the dark for 6 hours. After completion of the reaction, the solvent was evaporated under reduced pressure, and the resulting residue was analyzed by gas chromatography with a flame-ionization detector (GC-FID) and .sup.1H NMR. There was no reaction observed, and original substrate could be recovered after the reaction. This confirmed that light irradiation is essentially required for the activation of CO.sub.2 to provide necessary oxygen for the oxidation reaction.

Example 4

Oxidation of Benzaldehyde without CO.SUB.2

[0057] Benzaldehyde (1a) and polar organic solvent, preferably acetonitrile (1:2 to 1:10 weight ratio with respect to the substrate) was taken into a 60-mL vessel. The reaction mixture was purged with N.sub.2 in place of CO.sub.2. The reaction vessel was sealed and irradiated with a 20-W LED light for 6 hours. After completion of the reaction, the solvent was evaporated under reduced pressure, and the resulting residue was analyzed by GC-FID and .sup.1H NMR. There was no reaction observed, and the original substrate could be recovered after the reaction. This confirmed that the required oxygen for the oxidation of benzaldehyde was derived from carbon dioxide.

Example 5

Oxidation of Benzaldehyde Using Different Solvents

[0058] Benzaldehyde (1a) and an organic solvent (1:2 to 1:10 weight ratio with respect to the substrate) were taken into a 60-mL vessel. The reaction mixture was saturated with CO.sub.2 by purging. The reaction vessel was sealed and irradiated with a 20-W LED light for 2 hours. The intensity of the LED light at the reaction flask was measured to be 86 W/m.sup.2 by intensity meter. After completion of the reaction, the solvent was evaporated under reduced pressure, and the resulting residue was subjected to column chromatography on a silica gel (100-200 mesh) column using a 9:1 hexane—ethyl acetate solvent mixture as an eluent to afford pure benzoic acid. The results of the experiments in different solvents are summarized in Table 1, entries 1 and 5-9.

Example 6

Oxidation of Different Aldehydes Under Optimized Conditions

[0059] Aldehyde (1b-1h) and polar organic solvent, preferably acetonitrile (1:2 to 1:10 weight ratio with respect to the substrate) was taken into a 60-mL vessel. The reaction mixture was saturated with CO.sub.2 by purging. The reaction vessel was sealed and irradiated with 20-W LED light for 2 hours to 10 hours. The intensity of the LED light at the reaction flask was measured to be 86 W/m.sup.2 by intensity meter. The progress of the reaction was monitored by thin-layer chromatography using silica gel. After completion of the reaction, the solvent was evaporated under reduced pressure and the resulting residue was subjected to column chromatography on a silica gel (100 to 200 mesh) column using a 9:1 hexane—ethyl acetate solvent mixture as an eluent to afford pure acid. The isolated yields and the reaction times of these experiments are summarized in Table 1, entries 10-19.

TABLE-US-00001 TABLE 1 Photochemical oxidation of aldehydes with CO.sub.2 React, No. Aldehyde Acid time (h) Solvent Yield  1 Benzaldehyde (1a) Benzoic acid (2a) 2 CH.sub.3CN 96%.sup.a  2.sup.c Benzaldehyde (1a) Benzoic acid (2a) — CH.sub.3CN 75%.sup.a  3.sup.d Benzaldehyde (1a) — 6 CH.sub.3CN —  4.sup.e Benzaldehyde (1a) — 6 CH.sub.3CN —  5 Benzaldehyde (1a) Benzoic acid (2a) 2 DMA 78%.sup.a  6 Benzaldehyde (1a) Benzoic acid (2a) 2 DMF 75%.sup.a  7 Benzaldehyde (1a) Benzoic acid (2a) 2 DMSO (55%).sup.b  8 Benzaldehyde (1a) Benzoic acid (2a) 2 NMP (20%).sup.b  9 Benzaldehyde (1a) Benzoic acid (2a) 2 H.sub.2O (45%).sup.b 10 4-methylbenzaldehyde (1b) 4-methylbenzoic acid (2b) 4 CH.sub.3CN 97%.sup.a 11 4-methoxybenzaldehyde (1c) 4-methoxybenzoic acid (2c) 6 CH.sub.3CN 95%.sup.a 12 4-chlorobenzaldehyde (1d) 4-chlorobenzoic acid (2d) 10 CH.sub.3CN 85%.sup.a 13 3,4-dichlorobenzaldehyde (1e) 3,4-dichloro-benzoic acid (2e) 10 CH.sub.3CN 72%.sup.a 14 4-nitrobenzaldehyde (1f) 4-nitrobenzoic acid (2f) 12 CH.sub.3CN (30%).sup.b 15 Furan-2-carboxaldehyde (1g) Furan-2-carboxylic acid (2g) 12 CH.sub.3CN (51%).sup.b 16 2-thiophene-carboxylic acid (1h) 2-thiophene-carboxylic acid (2h) 12 CH.sub.3CN (52).sup.b 17 3,4-dimethoxybenzaldehyde (1i) 3,4-dimethoxy-benzoic acid (2i) 10 CH.sub.3CN (40%).sup.b 18 2-methylbenzaldehyde (1j) 2-methyl benzoic acid (2j) 6 CH.sub.3CN (42%).sup.b 19 Cinnamaldehyde (1k) Cinnamic acid (2k) 12 CH.sub.3CN (36%).sup.b .sup.aIsolated yield; .sup.bYield based on recovered aldehyde; .sup.cIn a flow photoreactor; .sup.dUnder dark conditions; .sup.eWithout CO.sub.2, under N.sub.2.

[0060] Accordingly, embodiments herein provide a catalyst-free light assisted utilization of CO.sub.2 for chemical synthesis.

[0061] Embodiments herein further provide a catalyst-free photochemical synthesis of carboxylic acids from oxidation of aldehydes using CO.sub.2 as an oxidant under ambient temperature and pressure conditions. The use of CO.sub.2 as an oxidant offer several advantages as it is abundantly available, safe, and inexpensive; also it provided carbon monoxide, an important building block as a co-product during the oxidation process.

[0062] Using benzaldehyde and its derivatives substituted with electron donating groups as substrates the conversion and yield of the corresponding acids remained higher than the substrates having electron withdrawing groups.

[0063] The best results were obtained in acetonitrile solvent; whereas, DMF and DMA being a CO.sub.2-philic solvent showed moderate reactivity.

[0064] The processes disclosed herein provide a viable approach that can serve as a tool for chemical fixation of CO.sub.2 in a sustainable way under mild operating conditions.