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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444392Generated: October 30, 2026

2-Aminothiophenol → HCID 12878966, compound

https://huagongshe.com/reaction/444392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantHCID 86737707HCID 86737707—
SolventEthanolHCID 702—
ProductHCID 12878966HCID 1287896627.4%

Reaction Steps

A mixture of 32 g of o-aminothiophenol, 69.6 g of ethyl p-methoxybenzalmalonate and 1.6 g of triethylamine hydrochloride was heated at about 180° C. until no further ethanol was distilled out (for about 4 hours). The resulting mixture was then worked up in the same manner as described in Reference Example 2 (a) and the crystals thus obtained were recrystallized from chloroform-petroleum ether to obtain 25 g of 2,3-dihydro-3-ethoxycarbonyl-2-(p-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one as colorless needles having a melting point of 192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264497
Source datasetuspto-grants-1981_04
ORD IDord-3a6c47db368f469694ed4994ce6f1e1b
Source noteuspto-grants-1981_04