Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439865Generated: October 26, 2026

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

https://huagongshe.com/reaction/1439865

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 numberUS05496815
Source datasetuspto-grants-1996_03
ORD IDord-5e2a977b30994d0bba62d64549e513b5
Source noteuspto-grants-1996_03