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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1439865Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1439865

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiophenolHCID 8713—
EduktSodium AcetateHCID 517045—
EduktMethyl 2-bromo-2-(4-fluorophenyl)acetateHCID 12717580—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 1369076187,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05496815
Quelldatensatzuspto-grants-1996_03
ORD IDord-5e2a977b30994d0bba62d64549e513b5
Quellennotizuspto-grants-1996_03