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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182087Generated: November 2, 2026

1-Chloroethyl chloroformate → Azetidin-3-yl(4-chlorophenyl)methanone hydrochloride

https://huagongshe.com/reaction/1182087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant(1-Benzhydryl-azetidin-3-yl)-(4-chloro-phenyl)-methanoneHCID 69361102—
SolventDichloromethaneHCID 6344—
ProductAzetidin-3-yl(4-chlorophenyl)methanone hydrochlorideHCID 69358091—

Reaction Steps

A solution of (1-Benzhydryl-azetidin-3-yl)-(4-chloro-phenyl)-methanone (19.8 g, 54.8 mmol) in dichloromethane (250 ml), cooled to −4° C., is treated with 1-chloroethylchloroformate (8.0 ml, 73.8 mmol) and allowed to warm to ambient temperature. The reaction mixture is stirred for 18 hours and then evaporated. The residue is dissolved in methanol (220 ml) and stirred at ambient temperature for 3.5 hours. The methanol solution is concentrated and the product precipitated by addition of diethylether. The precipitate is collected by filtration and dries under high vacuum to afford Azetidin-3-yl-(4-chloro-phenyl)-methanone hydrochloride. [MH]+ 195.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288537B2
Source datasetuspto-grants-2007_10
ORD IDord-650a3f69dbc245e8888a830ff0612043
Source noteuspto-grants-2007_10