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HRID 423182作成日:2026年10月25日

Sodium borohydride → (3-Bromopyridin-2-yl)methanol

https://huagongshe.com/reaction/423182

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物Methyl 3-bromo-2-pyridinecarboxylateHCID 12828946—
溶媒MethanolHCID 887—
生成物(3-Bromopyridin-2-yl)methanolHCID 1402252162%

反応条件

温度0 °C

反応手順

3-Bromo-pyridine-2-carboxylic acid methyl ester (12.8 g, 59.2 mmol) is dissolved in methanol (150 mL) and cooled to 0° C. To the mixture is added NaBH4 (11.2 g, 296 mmol) in 1.0 g portions. The mixture is warmed to room temperature and stirred for 3 h. The methanol is removed under reduced pressure, AcOEt is added and the solution is washed with saturated, aqueous ammonium chloride and brine. The organic portion is dried over MgSO4, filtered, and concentrated under reduced pressure to yield 6.8 g (62%) of the title compound as a white solid. GCMS m/e 187 [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101761B2
出典データセットuspto-grants-2012_01
ORD IDord-90478131fd2643e281544e934bd8959d
出典メモuspto-grants-2012_01