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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691031Generated: November 2, 2026

Thionyl Chloride → 2-Chloro-6-(chloromethyl)pyridine

https://huagongshe.com/reaction/1691031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-Chloropyridin-2-yl)methanolHCID 182139—
ReactantSodium BicarbonateHCID 516892—
SolventTolueneHCID 1140—
Product2-Chloro-6-(chloromethyl)pyridineHCID 1557444073%

Reaction Steps

To a mixture of (6-chloro-pyridine-2-yl)-methanol (200 mg, 1.39 mmol) described in Manufacturing Example 52-1-1 and toluene (3 mL) was added thionyl chloride (152 μL, 2.09 mmol) on an ice bath, which was stirred for 2 hours at room temperature. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, which was then extracted with ethyl acetate. 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, and the residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=4:1) to obtain the title compound (163.2 mg, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-c4be256d971349ce8ac606e3c1485982
Source noteuspto-grants-2012_04