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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207142Generated: October 30, 2026

3-Bromopyridine-4-carboxaldehyde → (3-Bromopyridin-4-yl)methanol

https://huagongshe.com/reaction/2207142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromopyridine-4-carboxaldehydeHCID 2762997—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(3-Bromopyridin-4-yl)methanolHCID 46840038100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-bromo-4-pyridinecarboxaldehyde 3 (3.0 g, 16.2 mmol) in absolute methanol (40 mL) was added NaBH4 (0.736 g 19.5 mmol) at 0° C. The mixture was stirred at 0° C. for 2 hours under nitrogen. The solvent was then removed under vacuum. Water and ethyl acetate were added and the organic layer was washed with water, dried over Na2SO4 and evaporated under vacuum to afford the compound 4 (3.021 g, 100%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376387B2
Source datasetuspto-grants-2016_06
ORD IDord-bb7c78d3d0b540f092a6812cd00b00eb
Source noteuspto-grants-2016_06