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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693847Generated: November 1, 2026

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

https://huagongshe.com/reaction/1693847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Fluoropyridin-2-yl)methanolHCID 24729312—
SolventDichloromethaneHCID 6344—
Product2-(Chloromethyl)-5-fluoropyridineHCID 2169805970.4%

Reaction Steps

To a solution of (5-fluoro-pyridin-2-yl)-methanol (945 mg, 7.43 mmol) described in Manufacturing Example 41-1-1 in methylene chloride (70 mL) was added dropwise thionyl chloride (813 μL, 11.1 mmol) at room temperature, which was stirred for 30 minutes. This reaction solution was partitioned by addition of water, sodium hydrogencarbonate and methylene chloride. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (hexane:diethyl ether=1:1) to obtain the title compound (761.1 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-5ae6e76f14814f7a9197dc28c42c1851
Source noteuspto-grants-2012_04