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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661629Generated: October 30, 2026

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

https://huagongshe.com/reaction/1661629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromopyridine-4-carboxaldehydeHCID 2762997—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(3-Bromopyridin-4-yl)methanolHCID 46840038—

Reaction Steps

To a solution of 3-bromo-pyridine-4-carbaldehyde (0.500 g, 2.68 mmol) in MeOH (5 mL) at 0° C. is added sodium borohydride (0.122 g, 3.22 mmol). The mixture is stirred at room temperature for 1 h followed by removal of the solvent in vacuo. The residue is redissolved in DCM and washed with water twice. The organic layer is dried over sodium sulfate and concentrated in vacuo to afford (3-bromo-pyridin-4-yl)-methanol as a yellow oil. MS (ESI) m/z 189.9 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-cddba3c5050640ad92b07b0b58adb2f3
Source noteuspto-grants-2011_10