Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706476Generated: October 30, 2026

4-Chlorobenzoyl chloride → HCID 23453038, compound

https://huagongshe.com/reaction/1706476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantEthyl 4-(2-aminoethyl)benzeneacetateHCID 20463409—
SolventPyridineHCID 1049—
ProductHCID 23453038HCID 2345303870%

Reaction Conditions

Temperature10 °C

Reaction Steps

8.3 g 4-Chlorobenzoyl chloride are added dropwise at 5°-10° C., within the course of 10 minutes, to a solution of 11.0 g ethyl 4-(2-aminoethyl)-phenylacetate in 90 ml anhydrous pyridine. The reaction mixture is then stirred for 90 minutes at 10° C., subsequently allowed to warm up to 20° C. and thereafter warmed to 40°-45° C. for 30 minutes. The reaction mixture is then cooled and stirred into 900 ml ice water, a solid precipitate thereby being obtained. This is filtered off with suction and washed with water. There are obtained 14.5 g (94% of theory) of crude product which is recrystallized from isopropanol to give 10.9 g (70% of theory) ethyl 4-[2-(4-chlorobenzamido)-ethyl]-phenylacetate; m.p. 118°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207341
Source datasetuspto-grants-1980_06
ORD IDord-d0866f12fbdc4f349a53cebcac96a756
Source noteuspto-grants-1980_06