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HRID 530011作成日:2026年10月27日

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

https://huagongshe.com/reaction/530011

反応式

関与物質

役割名称HCID仕込み量
反応物3-Acetyl-5-bromopyridineHCID 820423—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物2-(5-Bromo-3-pyridyl)propan-2-olHCID 22391966—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09351973B2
出典データセットuspto-grants-2016_05
ORD IDord-78161fb62e904e78b4b4173b12300011
出典メモuspto-grants-2016_05