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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443289Generated: October 30, 2026

Thionyl Chloride → 2-(Benzyloxy)-6-(chloromethyl)pyridine

https://huagongshe.com/reaction/443289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-(Benzyloxy)pyridin-2-yl)methanolHCID 21193214—
SolventBenzeneHCID 241—
Product2-(Benzyloxy)-6-(chloromethyl)pyridineHCID 21193174—

Reaction Steps

A mixture of 2-benzyloxy-6-hydroxymethylpyridine (1.5 g, 7.0 mmol) and thionyl chloride (10 mL, 137 mmol) in benzene (25 mL) was stirred at room temp. overnight. The product mixture was concentrated under vacuum. The residue was partitioned between chloroform and aqueous sodium bicarbonate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 5% methanol in chloroform. Collection and concentration of appropriate fractions provided 2-benzyloxy-6-chloromethylpyridine as clear, colorless oil. This alkylating reagent was passed through a small plug of activated basic alumina immediately before use.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-b1199d2dc1974ab89c405153a163004d
Source noteuspto-grants-1999_04