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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5842생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiophenolHCID 8713—
반응물Sodium AcetateHCID 517045—
반응물Methyl 2-bromo-2-(4-fluorophenyl)acetateHCID 12717580—
용매EthanolHCID 702—
생성물2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 1369076187.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246929
출처 데이터셋uspto-grants-1993_09
ORD IDord-c9f7e092e3be4773aba7a95c56f0342d
출처 메모uspto-grants-1993_09