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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243812Generated: November 1, 2026

Benzyl Alcohol → 2-Benzyloxy-6-cyano-3-methylpyridine

https://huagongshe.com/reaction/1243812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-5-methylpyridine-2-carbonitrileHCID 21928322—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Benzyloxy-6-cyano-3-methylpyridineHCID 2192830552%

Reaction Steps

To a solution of 2-bromo-6-cyano-3-methylpyridine (272 mg) and benzyl alcohol (156 mg) in tetrahydrofuran (20 mL) was added sodium hydride (40 mg), and the mixture was heated under reflux for one hour. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed successively with saturated aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. After removal of the sodium sulfate by filtration, the organic solvent was evaporated off in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=19:1) to give the title compound (161 mg) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119107B2
Source datasetuspto-grants-2006_10
ORD IDord-049107b3004541678c41d2d7cd3017b8
Source noteuspto-grants-2006_10