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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075552Generated: October 30, 2026

Sodium borohydride → 6-Bromo-3-pyridinemethanol

https://huagongshe.com/reaction/2075552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
SolventMethanolHCID 887—
Product6-Bromo-3-pyridinemethanolHCID 642124998.5%

Reaction Steps

To a solution of 4.85 g of 6-bromo-pyridine-3-carboxaldehyde in 50 mL of MeOH at 0° C. was added 1.93 g of NaBH4. This mixture was allowed to warm to room temperature. Upon completion of the reaction, the reaction mixture was concentrated to a residue, which was partitioned between ethyl acetate and water and extracted with ethyl acetate. The organic layer was washed with brine and dried over sodium sulphate. Purification by flash chromatography (silica, heptanes/ethyl acetate) provided 4.83 g of (6-bromo-pyridin-3-yl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-237772472e3043e1a49f0fd9240e2f53
Source noteuspto-grants-2011_04