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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476680Generated: October 30, 2026

Acetyl chloride → 1-Methyl 2-carboxybenzenepropanoate

https://huagongshe.com/reaction/476680

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 numberUS04885313
Source datasetuspto-grants-1989_12
ORD IDord-297e8aa287434ff09466f2c5eced29e4
Source noteuspto-grants-1989_12