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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443279Generated: October 26, 2026

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

https://huagongshe.com/reaction/443279

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 numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-000206fc93154c64a5aedfe76e8d6694
Source noteuspto-grants-1999_04