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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861379Generated: October 30, 2026

Benzyl Alcohol → 4-(Benzyloxy)pyridine

https://huagongshe.com/reaction/861379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant4-ChloropyridineHCID 12288—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
Product4-(Benzyloxy)pyridineHCID 1232882895%

Reaction Steps

To a suspension of sodium hydride (80% dispersed in oil, 876 mg, 29.2 mmol) in DMSO (10 ml) was added benzyl alcohol (3 ml, 29.2 mmol) and the mixture stirred at room temperature for 1 hour. To this was added 4-chloropyridine (3.3 g, 29.2 mmol) and the reaction stirred at room temperature overnight. The precipitated sodium chloride was removed by filtration and the filtrate diluted with water (100 ml) and extracted with ether (3×120 ml). The combined organic layers were dried (MgSO4) and evaporated in vacuo to yield the title compound as an oil (4.8 g, 95%); δH (CDCl3) 5.11 (2H, s, PhCH2O), 6.87 (2H, d, J 6.3 Hz, 3-H, 5-H), 7.29-7.42 (5H, m, Ph), and 8.42 (2H, d, J 6.3 Hz, 2-H, 6-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714498
Source datasetuspto-grants-1998_02
ORD IDord-8e1e4b65ad164f7ea1a076a8835be972
Source noteuspto-grants-1998_02