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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249631Generated: November 3, 2026

Oxalyl chloride → Ethyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoate

https://huagongshe.com/reaction/2249631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl 3-(2-isobutoxyphenyl)propanoateHCID 17816468—
Reactant2,5-Diisobutoxybenzoic acidHCID 17816477—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoateHCID 1781654898.4%

Reaction Steps

In 50 ml of methylene chloride is dissolved 5.00 g of 2,5-diisobutoxybenzoic acid. After adding 2.0 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, 7.51 g of aluminum chloride and subsequently 5.17 g of ethyl 3-(2-isobutoxyphenyl)-propanoate are added at −30° C., the mixture thus obtained is stirred at −10° C. for 10 minutes. The reaction mixture is added to a mixture of chloroform and ice 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 9.21 g of ethyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoate as a yellow-colored oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-bceb32f5e26e44adb92a08ab5636c1cd
Source noteuspto-grants-2008_01