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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249621Generated: October 31, 2026

Oxalyl chloride → Isobutyl 4-[3-(3-ethoxy-3-oxopropyl)-4-isobutoxybenzoyl]-3-isobutoxybenzoate

https://huagongshe.com/reaction/2249621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Isobutoxy-4-(isobutoxycarbonyl)-benzoic acidHCID 17816464—
ReactantEthyl 3-(2-isobutoxyphenyl)propanoateHCID 17816468—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductIsobutyl 4-[3-(3-ethoxy-3-oxopropyl)-4-isobutoxybenzoyl]-3-isobutoxybenzoateHCID 1781655365.2%

Reaction Steps

In 18 ml of methylene chloride is dissolved 1.8 g of 2-isobutoxy-4-(isobutoxycarbonyl)-benzoic acid. After adding 0.7 ml of oxalyl chloride and subsequently 20 μl of N,N-dimethylformamide at ambient temperature, the mixture thus obtained is stirred at ambient temperature for one hour. Then, 1.6 g of aluminum chloride and subsequently 1.8 g of ethyl 3-(2-isobutoxyphenyl)propanoate are added at 5-10° C., and the resulting mixture is stirred at ambient temperature for one hour. The reaction mixture is added to a mixture of chloroform and water and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 2.1 g of isobutyl 4-[3-(3-ethoxy-3-oxopropyl)-4-isobutoxybenzoyl]-3-isobutoxybenzoate as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-d6f0e9751f6441b18d8c115e936c58ad
Source noteuspto-grants-2008_01