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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068463Generated: October 31, 2026

Thionyl Chloride → 2-(Chloromethyl)-4-methylpyridine

https://huagongshe.com/reaction/1068463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4-Methylpyridin-2-yl)methanolHCID 12325388—
SolventBenzeneHCID 241—
Product2-(Chloromethyl)-4-methylpyridineHCID 12675261—

Reaction Steps

A mixture of 2-hydroxymethyl-4-methylpyridine (5.48 g, 44.5 mmol) and thionyl chloride (60 mL, 822 mmol) in benzene (150 mL) was stirred at room temp. overnight. The product mixture was concentrated under vacuum. The residue was partitioned between dichloromethane and aqueous sodium bicarbonate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under vacuum to provide the title compound as 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 numberUS06248756B1
Source datasetuspto-grants-2001_06
ORD IDord-109bb5e503ac44538bcd6509c4b4605b
Source noteuspto-grants-2001_06