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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896244Generated: November 1, 2026

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

https://huagongshe.com/reaction/1896244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-Methoxypyridin-3-yl)methanolHCID 12259941—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-2-methoxypyridineHCID 13752891216.1%

Reaction Steps

Thionyl chloride (0.23 ml, 3.23 mmol) was added to a solution of (6-methoxypyridin-3-yl)methanol (1.10 g, 8.41 mmol) in DCM at 0° C. and the reaction mixture was stirred for 2 h at room temperature. After completion of reaction, the volatiles were evaporated and the reaction mixture was basified with saturated sodium bicarbonate solution. The compound was extracted with DCM (2×30 ml) and washed with brine (15 ml). The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated and dried to afford 1.1 g (88%) of 5-(chloromethyl)-2-methoxypyridine as a colorless liquid. This compound was directly taken to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518948B2
Source datasetuspto-grants-2013_08
ORD IDord-58a2677de3c94effa800d4ef161ad027
Source noteuspto-grants-2013_08