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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470645Generated: November 1, 2026

Acetyl chloride → N-(2-Acetylphenyl)acetamide

https://huagongshe.com/reaction/1470645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2'-AminoacetophenoneHCID 11086—
Solvent1,1-DichloroethaneHCID 6365—
ProductN-(2-Acetylphenyl)acetamideHCID 21306—

Reaction Steps

To an ice cold slurry of the 1-(2-amino-phenyl)-ethanone (2 g, 14.79 mmol) in dichloroethane (10 mL), acetyl chloride (1.22 g, 16.2 mmol) was added slowly. The reaction mixture was warmed to room temperature and stirred for 2 h. After completion of the reaction, the reaction mixture was quenched with water (10 mL) and extracted with dichloromethane (2×25 mL). The combined organic layers were washed with an aq. solution of 5% NaHCO3 followed by water and brine, then dried over anhydrous sodium sulphate and concentrated to dryness. The obtained residue was purified by column chromatography using 2% ethyl acetate in hexane to obtain the title compound as off-white solid which directly used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006454B2
Source datasetuspto-grants-2015_04
ORD IDord-09431f2e228748049a20b97d96a03820
Source noteuspto-grants-2015_04