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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56469생성일: 2026년 10월 23일

Borohydride → (2-Amino-5-bromo-3-fluorophenyl)methanol

https://huagongshe.com/ko/reaction/56469

반응식

참여 물질

역할이름HCID투입량
반응물BorohydrideHCID 28123—
반응물2-Amino-5-bromo-3-fluorobenzoic acidHCID 40424597—
용매TetrahydrofuranHCID 8028—
생성물(2-Amino-5-bromo-3-fluorophenyl)methanolHCID 5431252595%

반응 단계

To a solution of 2-amino-5-bromo-3-fluorobenzoic acid (14.5 g, 62.2 mmol) in THF (150 mL) at 0° C. was added borohydride in THF (1 M, 310 mL), and the reaction mixture was stirred at room temperature overnight. The reaction was quenched with methanol (150 mL), concentrated in vacuum, diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL*3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (13.0 g, crude), which was directly used in the next step without the further purification. MS (ES+) C7H7BrFNO requires: 219, 221, found: 220, 222 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434700B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-cbaeea48176b456eaf135dbfa41aeec5
출처 메모uspto-grants-2016_09