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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839159Generated: November 1, 2026

Benzyl Alcohol → 2-Benzyloxy-5-bromopyridine

https://huagongshe.com/reaction/1839159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium HydroxideHCID 14797—
ReactantDibenzo-18-crown-6HCID 26541—
Reactant2,5-DibromopyridineHCID 69353—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Benzyloxy-5-bromopyridineHCID 11108191—

Reaction Steps

A mixture of 2,5-dibromopyridine, benzyl alcohol (1.3 eq), potassium hydroxide pellets (2.4 eq) and dibenzo-18-crown-6 (0.05 eq) in toluene (4 ml/mmol) was refluxed with azeotropic removal of water for 3 hours. After evaporation of the toluene, the resulting mixture was partitioned between chloroform and water. The crude product from the organic phase was recrystallized from ether-hexane to afford the 2-Benzyloxy-5-bromopyridine compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677351B2
Source datasetuspto-grants-2004_01
ORD IDord-0ab84277afc34d37a69b3a1109175b56
Source noteuspto-grants-2004_01