Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423208Generated: October 27, 2026

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

https://huagongshe.com/reaction/423208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 3-bromo-2-pyridinecarboxylateHCID 12828946—
SolventMethanolHCID 887—
Product(3-Bromopyridin-2-yl)methanolHCID 140225211,808.3%

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, ethyl acetate 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, 189 [M]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101760B2
Source datasetuspto-grants-2012_01
ORD IDord-29497b18e20f45bebc442b4fded9a82d
Source noteuspto-grants-2012_01