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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423182Generated: October 25, 2026

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

https://huagongshe.com/reaction/423182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 3-bromo-2-pyridinecarboxylateHCID 12828946—
SolventMethanolHCID 887—
Product(3-Bromopyridin-2-yl)methanolHCID 1402252162%

Reaction Conditions

Temperature0 °C

Reaction Steps

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]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101761B2
Source datasetuspto-grants-2012_01
ORD IDord-90478131fd2643e281544e934bd8959d
Source noteuspto-grants-2012_01