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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789634Generated: October 31, 2026

Acetyl chloride → 2'-Benzoylacetanilide

https://huagongshe.com/reaction/1789634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-AminobenzophenoneHCID 76080—
SolventDichloromethaneHCID 6344—
Product2'-BenzoylacetanilideHCID 97474—
Product2-Chloro-4-phenylquinolineHCID 2306687—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-4-phenylquinoline was prepared by the following method (Rxn-1). 2-Aminobenzophenone (21 g, 106.5 mmol) was dissolved in methylene chloride (213 mL) and triethylamine (22.3 mL, 159.8 mmol) was added slowly. After cooling to 0° C., acetylchloride (8.3 mL, 117.2 mmol) was added to the reaction mixture dropwise. The reaction mixture was then removed from ice and allowed to stir overnight. Upon the addition of 10% hydrochloric acid (84 mL), the aqueous layers were combined and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulfate, and concentrated. Purification by column chromatography (25% ethyl acetate/heptane) gave 2-acetamidobenzophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07070868B2
Source datasetuspto-grants-2006_07
ORD IDord-587fa6dd1dba43fda10d118c83fddfdf
Source noteuspto-grants-2006_07