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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618641Generated: October 30, 2026

Ethyl Thioglycolate → 6-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-one

https://huagongshe.com/reaction/1618641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-nitroanilineHCID 22691—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product6-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-oneHCID 4182356—

Reaction Steps

A solution of 2.44M aqueous NaOH (24 mL, 58 mmol) was added to a stirring solution of ethyl 2-mercaptoacetate (19 mL, 174 mmol) in EtOH (150 mL). The mixture was added to the stirring solution of 2-chloro-5-nitroaniline (10 g, 58 mmol) in EtOH (68 ml). The resulting mixture was heated at reflux overnight. After this time the reaction was diluted with EtOAc and washed with water. The separated organic layer was dried over Mg2SO4, filtered and evaporated in vacuo. The crude residue was triturated with EtOAc to give 6-nitro-2H-benzo[b]-[1,4]thiazin-3(4H)-one. Mass Spectrum (ESI) m/e=257 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-3c9c705aa7c74808b7bb55e0f8e63cf3
Source noteuspto-grants-2014_07