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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881494Generated: November 2, 2026

Sodium borohydride → (5-Bromopyridin-2-yl)methanol

https://huagongshe.com/reaction/881494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromopyridine-2-carbaldehydeHCID 9877562—
SolventMethanolHCID 887—
Product(5-Bromopyridin-2-yl)methanolHCID 5200169—

Reaction Steps

To a solution of 5-bromopyridine-2-carbaldehyde (300 mg) in methanol (10 mL) was added sodium borohydride (61 mg) and the reaction stirred at room temperature for 72 h. The reaction was quenched with saturated aqueous sodium carbonate solution (20 mL) and water (20 mL) and extracted into dichloromethane (3×30 mL). The organic layers were dried (MgSO4) and reduced in vacuo to give (5-bromo-pyridin-2-yl)-methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-2837ac9766f6442d9bad4d64a0c97964
Source noteuspto-grants-2015_03