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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220254Generated: November 2, 2026

Sodium borohydride → (6-o-Tolylpyridin-3-yl)methanol

https://huagongshe.com/reaction/2220254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-(2-Methylphenyl)pyridine-3-carbaldehydeHCID 24729662—
SolventEthanolHCID 702—
Product(6-o-Tolylpyridin-3-yl)methanolHCID 24729916100%

Reaction Steps

To a solution of 1.070 g (5.43 mmol) of 6-o-tolylnicotinaldehyde in 19 mL of ethanol at 0-5° C., was added 287 mg (7.5 mmol, 1.4 eq.) of sodium borohydride. After 2 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and, after 30 min, partitioned between dichloromethane and brine. The organic extract was dried over magnesium sulfate and concentrated to give the indicated product as a colorless oil, 1.08 g, 100% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-f84e07ea282143728995f2f0f4a60e0a
Source noteuspto-grants-2008_08