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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381614Generated: November 2, 2026

Acetyl chloride → 1-Methyl 2-carboxybenzenepropanoate

https://huagongshe.com/reaction/1381614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(2-Carboxyphenyl)propionic acidHCID 226294—
SolventDichloromethaneHCID 6344—
Product1-Methyl 2-carboxybenzenepropanoateHCID 11790422—

Reaction Steps

2-carboxybenzenepropanoic acid (9.7 g., 0.05 mole), acetic anhydride (15.5 g., 0.15 mole) and acetyl chloride (0.5 g) in dichloromethane (200 ml) was boiled at reflux under nitrogen for 16 hr. The solvents were removed at high vacuum and the residual cyclic anhydride was heated at reflux with methanol (250 ml) for 2 hrs. Evaporation of solvent gave the sub-title compound as an oil which crystallised with petroleum ether (b.p. 60°-80°) to a solid (6.3 g) mp 76°-79°. This was further purified by continuous extraction of the crude product with boiling petroleum (b.p. 40°-60°) in a Soxhlet apparatus. The pure compound, mp 79°-81° separated from the extracts on cooling.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803225
Source datasetuspto-grants-1989_02
ORD IDord-e166cd7f72b14d9eb0472c3d076836f3
Source noteuspto-grants-1989_02