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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376434생성일: 2026년 10월 25일

Benzoyl Peroxide → 1-(4-Fluoro-3-cyanophenyl)-3-trifluoromethyl-5-bromomethylpyrazole

https://huagongshe.com/reaction/376434

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물2-Fluoro-5-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzonitrileHCID 22280779—
용매Carbon TetrachlorideHCID 5943—
생성물1-(4-Fluoro-3-cyanophenyl)-3-trifluoromethyl-5-bromomethylpyrazoleHCID 2228079548.3%

반응 단계

To a solution of 1-(3-cyano-4-fluorophenyl)-3-trifluoromethyl-5-methyl pyrazole(4.0 g, 14.87 mmol) in carbon tetrachloride(50 mL) was added NBS(2.65 g, 14.87 mmol) and benzoyl peroxide(0.36 g, 1.48 mmol). The reaction mixture was brought to reflux overnight. Solvent was removed on rotary evaporator under reduced pressure. Residue was partitioned between ethyl acetate(80 mL) and sodium bicarbonate(sat. 80 mL). Organic phase was separated and washed with water(60 mL); dried over sodium sulfate; filtered, concentrated and subjected to silica-gel flash chromatography (ethyl acetate : hexane, 1:10) to afford 1-(3-cyano-4-fluorophenyl)-3-trifluoromethyl-5-bromomethyl pyrazole(2.5 g). CI mass spectrum m/z (rel. intensity) 348 (M+H, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020357
출처 데이터셋uspto-grants-2000_02
ORD IDord-f241532119f44f07a7e5cef7ea3a638e
출처 메모uspto-grants-2000_02