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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437905Generated: November 4, 2026

Thionyl Chloride → 3-(Chloromethyl)-2-methoxypyridine

https://huagongshe.com/reaction/1437905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2-Methoxypyridin-3-yl)methanolHCID 10630565—
SolventDichloromethaneHCID 6344—
Product3-(Chloromethyl)-2-methoxypyridineHCID 1493294586%

Reaction Steps

Thionyl chloride (9.5 mL, 130 mmol) was added portionwise to a solution of (2-methoxy-pyridin-3-yl)-methanol (1.02 g, 7.3 mmol) in dichloromethane (36 mL). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated and dichloromethane (100 mL) was added. The solution was carefully treated with saturated aqueous sodium hydrogen carbonate and the mixture was stirred for 5-10 min. The organic layer was separated and the aqueous layer was extracted with dichloromethane (2×100 mL). The combined organic layers were washed with brine (100 mL), dried (sodium sulfate), filtered, and evaporated to give 3-chloromethyl-2-methoxy-pyridine (989 mg, 86%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-af9f06699f5145d6bcda6a6ba6dd1620
Source noteuspto-grants-2009_11