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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715378Generated: October 30, 2026

Thionyl Chloride → 2-(Chloromethyl)-6-(2,2,2-trifluoroethoxy)pyridine

https://huagongshe.com/reaction/715378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-(2,2,2-Trifluoroethoxy)pyridin-2-yl)methanolHCID 62240732—
SolventDichloromethaneHCID 6344—
Product2-(Chloromethyl)-6-(2,2,2-trifluoroethoxy)pyridineHCID 62238846100.1%

Reaction Steps

A mixture of (6-(2,2,2-trifluoroethoxy)pyridin-2-yl)methanol (0.32 g, 1.55 mmol, Step-3), and thionyl chloride (0.23 mL, 3.10 mmol) in DCM (16 mL) is stirred at rt for 1 hour. The organic solvent is concentrated under reduced pressure and dried to give 0.35 g (>99% yield) of the title compound as yellow oil. This material is used for the next reaction (Step-5) without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187475B2
Source datasetuspto-grants-2015_11
ORD IDord-fedca559a2ba4649bcc36cf81ca3be0b
Source noteuspto-grants-2015_11