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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593584Generated: October 30, 2026

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

https://huagongshe.com/reaction/593584

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 numberUS09242963B2
Source datasetuspto-grants-2016_01
ORD IDord-196e5af2399b48d5b099b41a5f155237
Source noteuspto-grants-2016_01