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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2353459생성일: 2026년 10월 27일

N-bromobutanimide → 5-bromo-7-fluoro-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/2353459

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참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물7-Fluoro-2,3-dihydro-1H-indoleHCID 16768261—
용매AcetonitrileHCID 6342—
생성물5-bromo-7-fluoro-2,3-dihydro-1H-indoleHCID 1679268960.7%

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온도0 °C

반응 단계

7-Fluoroindoline (1.1 g, 8.0 mmol) was dissolved in acetonitrile (80 mL), cooled to 0° C., and N-bromosuccinimide (1.43 g, 8.0 mmol) was added. The mixture was warmed to 25° C. and stirred for 3 hours. The mixture was concentrated to 10 mL and diluted with ethyl acetate and washed with NaHCO3, water, brine, dried over anhydrous magnesium sulfate, and concentrated. Purification via Isco chromatography (the Redisep® column, silica, gradient 5%-15% ethyl acetate in hexane) afforded 5-bromo-7-fluoroindoline (1.05 g). MS (ES) m/z 215.8; HPLC purity 97.6% at 210-370 nm, 10.5 min.; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammonium formate buffer pH=3.5 acetonitrile+MeOH) for 10 minutes, hold 4 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07750038B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-a05fd7e085104285a8551e12552e941c
출처 메모uspto-grants-2010_07