Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524322Generated: November 1, 2026

Thionyl Chloride → 2-Chloro-3-chloromethyl-pyridine

https://huagongshe.com/reaction/1524322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2-Chloropyridin-3-yl)methanolHCID 2763647—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product2-Chloro-3-chloromethyl-pyridineHCID 1152839989%

Reaction Steps

To a solution of the compound (18.5 g) obtained in step 1 in a mixture of chloroform (95 mL) and DMF (0.63 mL) was added thionyl chloride (14.0 mL) at 0° C., and the mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated under reduced pressure, and the residue was poured into a mixture of water and ethyl acetate. The solution was neutralized with sodium hydrogen carbonate, and the resultant product was extracted with ethyl acetate. The organic layer was washed with brine, and concentrated to give 2-chloro-3-(chloromethyl)pyridine (20.5 g, 89%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079907B2
Source datasetuspto-grants-2015_07
ORD IDord-941d562de62d47d9a59141d90f283c74
Source noteuspto-grants-2015_07