Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693876Generated: November 1, 2026

Thionyl Chloride → 4-Chloro-2-(chloromethyl)pyridine

https://huagongshe.com/reaction/1693876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Chloropyridin-2-yl)methanolHCID 2763167—
SolventTolueneHCID 1140—
Product4-Chloro-2-(chloromethyl)pyridineHCID 1305290159.9%

Reaction Steps

To a mixture of (4-chloro-pyridine-2-yl)-methanol (146.8 mg, 1.0 mmol) described in Manufacturing Example 51-1-1 and toluene (3 mL) was added thionyl chloride (112 μL, 1.53 mmol) on an ice bath, which was stirred for 1 hour 15 minutes 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 (97 mg, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-f82b52dd839a4d3a9071764064fef260
Source noteuspto-grants-2012_04