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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493393Generated: October 30, 2026

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

https://huagongshe.com/reaction/493393

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 numberUS07534763B2
Source datasetuspto-grants-2009_05
ORD IDord-be46d817115f47078c09952a97e3d274
Source noteuspto-grants-2009_05