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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5842Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/5842

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 1369076187.6%

Reaction Steps

To a suspension of 2-aminothiophenol (12.6 g) and 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 g) as crystals. M.p. 216°-219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246929
Source datasetuspto-grants-1993_09
ORD IDord-c9f7e092e3be4773aba7a95c56f0342d
Source noteuspto-grants-1993_09