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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263104Generated: October 28, 2026

4-Chlorobenzoyl chloride → HCID 131711511, compound

https://huagongshe.com/reaction/263104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 20298675HCID 20298675—
SolventChloroformHCID 6212—
ProductHCID 131711511HCID 131711511—

Reaction Steps

A solution of 16.0 g. of 4-[3-[4-methoxy-2-[[(2-phenylethyl)amino]methyl]phenoxy]propyl]morpholine in 50 ml. of chloroform is added dropwise (at 10°-15° C.) to a stirred solution of 7.7 g of p-chlorobenzoyl chloride in 150 ml. of chloroform. After the addition is completed, the solution is stirred at room temperature for 2 hours, heated at reflux for 1 hour, cooled and concentrated to give a glass-like residue. The residue is rubbed under ether, the evaporation repeated and the partly solid residue taken up in 100 ml of acetonitrile. On diluting to 650 ml with ether, seeding and rubbing, the crystalline hydrogen chloride salt separates. After cooling overnight, the product weighs 21.7 g, melting point 137°-139° C. Recrystallization from 50 ml of warm acetonitrile-50 ml of ether, yields 20.3 g of the title compound, melting point 138°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04156079
Source datasetuspto-grants-1979_05
ORD IDord-78c93932c1b44d45a229525336682917
Source noteuspto-grants-1979_05