Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693778Generated: November 2, 2026

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

https://huagongshe.com/reaction/1693778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4-Methylpyridin-2-yl)methanolHCID 12325388—
SolventDichloromethaneHCID 6344—
Product2-(Chloromethyl)-4-methylpyridineHCID 1267526172.1%

Reaction Steps

A mixture solution of (4-methyl-pyridine-2-yl)-methanol (410 mg, 3.33 mmol) described in Manufacturing Example 11-1-3, thionyl chloride (0.49 mL, 6.66 mmol) and methylene chloride (10 mL) was stirred under reflux for 5 minutes. The reaction solution was allowed to room temperature and concentrated under a reduced pressure. The resulting residue was partitioned into diethyl ether and saturated sodium bicarbonate solution. The organic layer was purified by silica gel column chromatography (ethyl acetate) to obtain the title compound (340 mg, 72.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-22ca8f62d3964d7d9cd4c9edbbc67065
Source noteuspto-grants-2012_04