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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588030Generated: October 31, 2026

Acetic Anhydride → N-Acetyl-3-nitrobenzamide

https://huagongshe.com/reaction/1588030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-NitrobenzamideHCID 12576—
SolventDichloromethaneHCID 6344—
ProductN-Acetyl-3-nitrobenzamideHCID 19756873—

Reaction Steps

A solution of 3-nitrophenylcarboxamide (2 g) in 125 ml of dry methylene chloride was cooled to 0° C. and mixed with 1.25 ml of acetic anhydride and 2.1 g of 4-N,N-dimethylaminopyridine. The reaction mixture was warmed to room temperature and stirred for 1 hour. Additional amounts of 4-N,N-dimethylaminopyridine (809 mg) and acetic anhydride (1.25 ml) were added to the reaction mixture and stirring was continued overnight. The reaction mixture was diluted with 300 ml of methylene chloride and was washed with 60 ml of 5% citric acid solution. The organic extracts were dried, concentrated in vacuo, and the residue was chromatographed on silica gel (chloroform-methanol, 97:3 v/v) to yield 500 mg of the title compound in pure form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05220018
Source datasetuspto-grants-1993_06
ORD IDord-e3bf2dacc70641d8a5b5e65fc9e17504
Source noteuspto-grants-1993_06