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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834065Generated: October 31, 2026

Methanol → HCID 21388463, compound

https://huagongshe.com/reaction/1834065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 16226924HCID 16226924—
ReactantHCID 21388449HCID 21388449—
SolventBenzeneHCID 241—
ProductHCID 21388463HCID 21388463—

Reaction Steps

In a 100-ml. three necked flask was placed 11.5 g. of N-(α-cyano-4-methoxybenzyl)piperazine and 40 ml. of methanol to obtain a homogenous solution. To the resulting solution was added dropwise 5.96 g. of ethyl chloroformate over a period of about 70 minutes with stirring while the temperature was kept at about 20° C. After dropping, the internal temperature was raised to 40° to 45° C., and then the mixture was further stirred for 2 hours. The solution was concentrated under reduced prossure and 500 ml. of water was added thereto. This solution was made alkaline with the aid of sodium carbonate with cooling and extracted with benzene. The benzene layer was washed with dilute hydrochloric acid and water, and dried over sodium sulfate. The solvent was distilled off to afford 9.7 g. of N-(α-cyano-4-methoxybenzyl)-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-methoxybenzyl)-N'-ethoxycarbonylpiperazine hydrochloride having a melting point of 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04068070
Source datasetuspto-grants-1978_01
ORD IDord-058a03cd51b24fff97981d88db6243a3
Source noteuspto-grants-1978_01