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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276014Generated: October 27, 2026

Hydrochloric Acid → ethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoate

https://huagongshe.com/reaction/276014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantalpha-Bromo-o-chlorotolueneHCID 11905—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-acetylamino-4-nitrobenzoateHCID 18315393—
SolventDimethylformamideHCID 6228—
Productethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoateHCID 1831554981.6%

Reaction Steps

A solution of 1.706 g of ethyl 3-acetylamino-4-nitrobenzoate in 12 ml of N,N-dimethylformamide were added 0.406 g of 60% sodium hydride while being cooled with ice, and the mixture was stirred at room temperature for 40 minutes. A solution of 1.806 g of 2-chlorobenzyl bromide in 10 ml of N,N-dimethylformamide was added thereto, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into cold 1-N hydrochloric acid, and the mixed solution was extracted twice with ethyl acetate. The organic layer was washed with 1-N hydrochloric acid and then with water, and was dried. The solvent was distilled off under reduced pressure. The residue was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and hexane at a ratio of from 1:10 to 1:4) to give 2.08 g of oily ethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-86bbd89d855f442c8e9f95991ba4ccc3
Source noteuspto-grants-2002_03