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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991430Generated: November 2, 2026

Benzoic acid, 4-(acetyloxy)- → p-Acetoxybenzoyl chloride

https://huagongshe.com/reaction/991430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 4-(acetyloxy)-HCID 16865—
ReactantOxalyl chlorideHCID 65578—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productp-Acetoxybenzoyl chlorideHCID 2756254—

Reaction Conditions

Temperature0 °C

Reaction Steps

Oxalyl chloride (0.35 ml) was added to a stirred suspension of 4-acetoxybenzoic acid (0.57 g) in methylene chloride (15 ml) which had been cooled to 0° C. DMF (2 drops) was added and the mixture was stirred at ambient temperature for 4 hours. The mixture was evaporated to give 4-acetoxybenzoyl chloride which was used without further purification. A mixture of the acid chloride so obtained, N-(3-amino-4-chlorophenyl)-4-cyanobenzamide (0.813 g) and pyridine (15 ml) was stirred and heated at 100° C. for 16 hours. The mixture was cooled to ambient temperature and poured into 2N aqueous hydrochloric acid solution (175 ml). The precipitate was isolated, washed with water and dried. The material so obtained was purified by column chromatography on silica using a 7:3 mixture of isohexane and ethyl acetate as eluent. There was thus obtained the title compound (0.74 g); m.p. 195-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465455B1
Source datasetuspto-grants-2002_10
ORD IDord-bf438f129d634d4c9cb247d55e48924b
Source noteuspto-grants-2002_10