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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231206Generated: October 31, 2026

Chloroacetyl chloride → HCID 14257921, compound

https://huagongshe.com/reaction/2231206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant68770-54-7HCID 20396933—
SolventChloroformHCID 6212—
SolventCyclohexaneHCID 8078—
ProductHCID 14257921HCID 1425792174.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

Triethylamine (254.9 g, 2.5 mol) was added with stirring to a solution of 1-phenyl-2-(3-methoxyphenyl)ethylamine hydrochloride (166.0 g, 0.63 mol) in chloroform (4 L) under nitrogen at 0° C. Then chloroacetyl chloride (142.2 g, 1.26 mol) was added dropwise over a period of 2 hrs. The resulting mixture was stirred at ambient temperature (about 25° C.) for 16 hrs, washed with 10% HCl (3×1 L) and water (1 L), and then the organic phase was dried over MgSO4. Evaporation of the solvent gave a dark oily residue which was dissolved in cyclohexane (2 L). Upon standing, the resulting solution gave solid crystals which were collected by filtration and dried to give 142.5 g of N-chloroacetyl-1-phenyl-2-(3-methoxyphenyl)ethylamine. A sample recrystallized twice from cyclohexane had a mp. 104°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782058
Source datasetuspto-grants-1988_11
ORD IDord-11cf446c102d4d4bbf6446e0f995196d
Source noteuspto-grants-1988_11