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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437902Generated: November 2, 2026

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

https://huagongshe.com/reaction/1437902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-Methoxypyridin-3-yl)methanolHCID 12259941—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-2-methoxypyridineHCID 1375289188%

Reaction Steps

Thionyl chloride (9.2 mL, 126 mmol) was added dropwise to a solution of (6-methoxy-pyridin-3-yl)-methanol (1.00 g, 7.2 mmol) in dichloromethane (38 mL). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated and dichloromethane (100 mL) was added. The solution was washed with saturated aqueous sodium hydrogen carbonate (this resulted in bubbling). The organic layer was separated and the aqueous layer was extracted with dichloromethane (2×100 mL). The combined organic layers were washed with brine (150 mL), dried (sodium sulfate), filtered, and evaporated to give 5-chloromethyl-2-methoxy-pyridine (995 mg, 88%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-2766b80c5634451c85a16c9089a92dda
Source noteuspto-grants-2009_11