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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198453Generated: October 26, 2026

2-Aminothiophenol → 2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-one

https://huagongshe.com/reaction/1198453

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantSodium AcetateHCID 517045—
ReactantMethyl 2-bromo-2-(4-fluorophenyl)acetateHCID 12717580—
SolventEthanolHCID 702—
Product2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 13690761—

Reaction Steps

To a suspension of 2-aminothiophenol (12.6 g) and o sodium acetate (23.6 g) in ethanol (150 ml) is added methyl α-bromo-4-fluorophenylacetate (23.6 g), and the mixture is stirred at room temperature overnight. After the solvent is distilled off, water is added to the residue. The resulting precipitate is separated by filtration, washed, dried, and then recrystallized from tetrahydrofuran-n-hexane to give 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (21.7 as crystals. M.p. 216°-219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281592
Source datasetuspto-grants-1994_01
ORD IDord-ad452b85b99c4164a124b711544a2b08
Source noteuspto-grants-1994_01