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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640175Generated: October 30, 2026

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

https://huagongshe.com/reaction/640175

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 numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-a4a7c76a64684614927a2a0f162b2d58
Source noteuspto-grants-2010_04