戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1439865作成日:2026年10月27日

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

https://huagongshe.com/reaction/1439865

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminothiophenolHCID 8713—
反応物Sodium AcetateHCID 517045—
反応物Methyl 2-bromo-2-(4-fluorophenyl)acetateHCID 12717580—
溶媒EthanolHCID 702—
生成物2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 1369076187.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05496815
出典データセットuspto-grants-1996_03
ORD IDord-5e2a977b30994d0bba62d64549e513b5
出典メモuspto-grants-1996_03