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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657780Generated: October 31, 2026

Pyridine → HCID 21388467, compound

https://huagongshe.com/reaction/1657780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 21388464HCID 21388464—
SolventDiethyl EtherHCID 3283—
ProductHCID 21388467HCID 21388467—

Reaction Steps

14.5 g. of N-(α-cyano-2,3,4-trimethoxybenzyl)piperazine was dissolved in 50 ml. of anhydrous diethyl ether and to the resultant solution was added 4 g. of pyridine. To the mixture was added dropwise 6 g. of ethyl chloroformate dissolved in 10 ml. of anhydrous diethyl ether over a period of about 30 minutes with ice cooling while the internal temperature was kept at 10° - 15°C. The mixture was further stirred at room temperature and filtered off to separate an insoluble matter. The filtrate was evaporated to give crude N-(α-cyano-2,3,4-trimethoxybenzyl)-N'-ethoxycarbonylpiperazine as an oily substance. This product was dissolved in toluene and the resultant solution was saturated with dry hydrochloric gas to separate crystal which was collected by filtration. Recrystallization from tetrahydrofuran-methanol afforded 14 g. of crystal having a melting point of 137.5° - 139.0°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962247
Source datasetuspto-grants-1976_06
ORD IDord-1a3447566e994eccb21d02010a159c7a
Source noteuspto-grants-1976_06