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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471240Generated: October 25, 2026

Benzyl Chloride → 2-(Benzyloxy)-6-chloropyridine

https://huagongshe.com/reaction/1471240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloropyridin-2-olHCID 178516025—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-6-chloropyridineHCID 1126446493.2%

Reaction Steps

To a flask were added 5.0 g 6-chloro-2-hydroxypyridine, 5.3 g potassium carbonate and 75 ml N,N-dimethylformamide. After cooling to 5 C under nitrogen, 5.9 g of benzyl chloride were added drop wise and the reaction mixture was warmed to 60 C for 3 hours. After cooling to 10 C, the reaction mixture was quenched with 75 ml of water and the product was extracted with ethyl acetate and washed with water. Following solvent removal, the product was purified by silica gel chromatography using 5% ethyl acetate in hexane to give a clear colorless oil 7.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09011734B2
Source datasetuspto-grants-2015_04
ORD IDord-f03e2f09d3db47349b11affb9d07dde9
Source noteuspto-grants-2015_04