돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662176생성일: 2026년 10월 27일

Methanol → N-((3-Bromo-4-fluorophenyl)(2-cyano-3-fluorophenyl)methylene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1662176

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-ButanesulfinamideHCID 3382465—
반응물2-(3-Bromo-4-fluoro-benzoyl)-6-fluoro-benzonitrileHCID 58579483—
촉매Titanium tetraethoxideHCID 76524—
용매TetrahydrofuranHCID 8028—
생성물N-((3-Bromo-4-fluorophenyl)(2-cyano-3-fluorophenyl)methylene)-2-methylpropane-2-sulfinamideHCID 7682160355%

반응 단계

2-(3-Bromo-4-fluoro-benzoyl)-6-fluoro-benzonitrile (7.9 g, 24.5 mmol) dissolved in dry THF (40 mL) was added to a solution of titanium (IV) ethoxide (12.7 ml, 61.3 mmol) in dry THF (30 mL) at room temperature. 2-Methyl-2-propanesulfinamide (3.57 g, 29.4 mmol) was added and the resulting mixture was heated at reflux temperature for 22 h. The reaction mixture was cooled to room temperature and methanol (120 mL) was added, followed by addition of saturated sodium bicarbonate (12 mL). The resulting suspension was filtered through a pad of sodium sulfate and the solids were washed thoroughly with ethyl acetate. The filtrate was concentrated in vacuo and purified by flash column chromatography using a gradient of 30-50% ethyl acetate in hexanes to afford 5.7 g (55% yield) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030500B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-b48e773ef98e438fa28a94f8d8d8d14d
출처 메모uspto-grants-2011_10