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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971164Generated: October 30, 2026

Oxalyl chloride → 2-(4-Chlorocarbonylphenyl)-2-methylpropionic acid methyl ester

https://huagongshe.com/reaction/971164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl 2-methyl-2-phenylpropanoateHCID 143498—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product2-(4-Chlorocarbonylphenyl)-2-methylpropionic acid methyl esterHCID 25111212—

Reaction Steps

To a suspension of AlCl3 (500.0 mg, 3.75 mmol) in CH2Cl2 at −10° C. was added dropwise oxalyl chloride (476.0 mg, 3.75 mmol) in CH2Cl2. The mixture was stirred at this temperature for 30 min. Then a solution of 2-methyl-2-phenyl-propionic acid methyl ester (178.0 mg, 1.0 mmol) in CH2Cl2 was added. The resulted mixture was stirred at −10° C. for 1 hr and rt overnight. The mixture was filtered through a pad of celite, the solvent and excess oxalyl chloride was removed under reduced pressure. The residue was dissolved in chlorobenzene and refluxed for 4 hr. Solvent was removed and the residue was dried to give 2-(4-chlorocarbonyl-phenyl)-2-methyl-propionic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312214B2
Source datasetuspto-grants-2007_12
ORD IDord-1ae7008a1fbb46c28dc5fd0759be2053
Source noteuspto-grants-2007_12