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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643281Generated: October 28, 2026

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

https://huagongshe.com/reaction/643281

Reaction equation

Participants

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

Reaction Conditions

Temperature0 °C

Reaction Steps

The 5-bromo-pyridine-2-carbaldehyde (2.0 g) was taken up in MeOH and cooled to 0° C. Sodium borohydride (450 mg) was added in portions at 0° C. The solution was warmed to 25° C. and stirred at that temperature for 1.5 h. The solution was concentrated, and the residue was quenched with 1 M HCl(aq.). The solution was stirred at 25° C. for 0.5 h. The solution was rendered basic via addition of solid K2CO3. The mixture was extracted with CH2Cl2. The combined organic layers were dried (MgSO4), filtered, and concentrated to give (5-bromo-pyridin-2-yl)-methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700597B2
Source datasetuspto-grants-2010_04
ORD IDord-8c0eefc32a6f4683815a241cef35359e
Source noteuspto-grants-2010_04