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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530011생성일: 2026년 10월 26일

3-Acetyl-5-bromopyridine → 2-(5-Bromo-3-pyridyl)propan-2-ol

https://huagongshe.com/reaction/530011

반응식

참여 물질

역할이름HCID투입량
반응물3-Acetyl-5-bromopyridineHCID 820423—
반응물HCID 178418573HCID 178418573—
용매TetrahydrofuranHCID 8028—
생성물2-(5-Bromo-3-pyridyl)propan-2-olHCID 22391966—

반응 조건

온도0 °C

반응 단계

Methyl magnesium bromide (5.3 mL, 0.075 mol) was added to a stirred solution of 1-(5-bromopyridin-3-yl)ethanone (1.0 g, 0.05 mol) in tetrahydrofuran (20.0 mL), cooled to 0° C. and the resulting mixture was allowed to warm to room temperature and stirred for 1.5 h. The reaction mixture was quenched with 1N hydrochloric acid (20 mL) and extracted with ethyl acetate (2×75 mL). The combined organic layers were dried over sodium sulphate and concentrated under vacuum to afford the crude compound which was purified by column chromatography to obtain 2-(5-bromopyridin-3-yl)propan-2-ol. MS (M+1): 217.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09351973B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-78161fb62e904e78b4b4173b12300011
출처 메모uspto-grants-2016_05