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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657782Generated: November 1, 2026

Ethyl chloroformate → HCID 21388470, compound

https://huagongshe.com/reaction/1657782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
Reactantα-(4-Chlorophenyl)-1-piperazineacetonitrileHCID 21388465—
ReactantHCID 21388468HCID 21388468—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 21388470HCID 21388470—

Reaction Steps

To 11.7 g. of N-(α-cyano-4-chlorobenzyl)piperazine was added 70 ml. of benzene and then 6.9 g. of anhydrous potassium carbonate. To the resulting solution was added dropwise 5.4 g. of ethyl chloroformate dissolved in 30 ml. of benzene with cooling. After dropping, the mixture was stirred for 2 hours at 40° - 45°C. After cooling, water was poured into the mixture to dissolve inorganic substance. The benzene layer was separated, washed with water, dried over sodium sulfate, and the solvent distilled off. There was obtained 10.7 g. of N-(α-cyano-4-chlorobenzyl)-N'-ethoxycarbonylpiperazine as an oily substance. This product was dissolved in benzene and the resultant solution was saturated with dry hydrochloric gas to separate crystal which was collected by filtration. Recrystallization from acetone afforded N-(α-cyano-4-chlorobenzyl)-N'-ethoxycarbonylpiperazine hydrochloride having a melting point of 166°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962247
Source datasetuspto-grants-1976_06
ORD IDord-5c62f18cb82d4f0f9db43bec1d5e405a
Source noteuspto-grants-1976_06