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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178570Generated: November 3, 2026

Benzyl Alcohol → 2-(Benzyloxy)-4-methylpyridine

https://huagongshe.com/reaction/1178570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-4-methylpyridineHCID 2734087—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(Benzyloxy)-4-methylpyridineHCID 1422347667%

Reaction Steps

Sodium hydride (60% paraffin dispersion, 5.0 g, 120 mmol) was washed with hexane (5 mL) twice and suspended in tetrahydrofuran (200 mL). To this suspension was added dropwise a solution of benzyl alcohol (14 g, 120 mmol) in tetrahydrofuran (50 mL) at 0° C. and then, the mixture was allowed to warm up to room temperature with stirring for 15 minutes. To this solution was added a solution of 2-bromo-4-methylpyridine (19.5 mL, 110 mmol) in tetrahydrofuran (50 mL) and heated to reflux for 14 hours. To the reaction mixture was added water (200 mL) and extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The crude product was distilled under reduced pressure to obtain 13 g of the title compound (67 mmol, yield 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276527B2
Source datasetuspto-grants-2007_10
ORD IDord-3026027910d644829784d3b5f40ad09f
Source noteuspto-grants-2007_10