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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444390Generated: November 1, 2026

Ethanol → HCID 12878956, compound

https://huagongshe.com/reaction/444390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-AminothiophenolHCID 8713—
ReactantHCID 23463634HCID 23463634—
CatalystPyridinium chlorideHCID 10176127—
ProductHCID 12878956HCID 12878956—

Reaction Steps

A mixture of 32 g of o-aminothiophenol, 70.7 g of p-chlorobenzalmalonate and 1.4 g of pyridine hydrochloride was heated at about 180° C. until no further ethanol was distilled out (for about 4 hours). After allowing the reaction mixture to cool, a mixture of benzene-petroleum ether was added to the reaction mixture which was then thoroughly stirred and filtered. The resulting filter cake was recrystallized from chloroform-petroleum ether to obtain 54.5 g of 2-(p-chlorophenyl)-2,3-dihydro-3-ethoxycarbonyl-1,5-benzothiazepin-4(5H)-one as colorless needles having a melting point of 206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264497
Source datasetuspto-grants-1981_04
ORD IDord-76aa82021c8d4430905b1e656bb666a1
Source noteuspto-grants-1981_04