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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629458Generated: October 29, 2026

Thionyl Chloride → 5-(Chloromethyl)-2-methylpyridine

https://huagongshe.com/reaction/629458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-Methylpyridin-3-yl)methanolHCID 11228788—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product5-(Chloromethyl)-2-methylpyridineHCID 1221433865.2%

Reaction Steps

To a solution of (6-methylpyridin-3-yl)methanol (1.08 g) in THF (15.0 mL) was added thionyl chloride (1.57 g) under ice-cooling, and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with water and ethyl acetate, saturated aqueous sodium bicarbonate was added thereto, and the mixture was partitioned. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.81 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315458B2
Source datasetuspto-grants-2016_04
ORD IDord-72124e27cf3d477883c3a99edb724c25
Source noteuspto-grants-2016_04