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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77962Generated: October 26, 2026

Thionyl Chloride → 5-Chloro-2-(chloromethyl)pyridine

https://huagongshe.com/reaction/77962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant(5-Chloropyridin-2-yl)methanolHCID 20537893—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-(chloromethyl)pyridineHCID 1451715178%

Reaction Steps

To a mixture of (5-chloro-pyridine-2-yl)-methanol (706 mg, 4.92 mmol) described in Manufacturing Example 63-1-1 and dichloromethane (70 mL) was added thionyl chloride (539 μL, 7.38 mmol), which was stirred for 1 hour at room temperature. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, which was then extracted with dichloromethane. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (620.0 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-d545fe424bee442cbd171484813d9857
Source noteuspto-grants-2014_09