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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666438Generated: October 31, 2026

Thionyl Chloride → 2-(3-(Chloromethyl)-5-ethoxyphenoxy)-5-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1666438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(3-Ethoxy-5-(5-(trifluoromethyl)pyridin-2-yloxy)phenyl)methanolHCID 66876312—
SolventDichloromethaneHCID 6344—
Product2-(3-(Chloromethyl)-5-ethoxyphenoxy)-5-(trifluoromethyl)pyridineHCID 66875661—

Reaction Steps

(3-Ethoxy-5-(5-(trifluoromethyl)pyridin-2-yloxy)phenyl)methanol from Step 2 (350 mg, 1.12 mmol), in dichloromethane (3 mL), was cooled to 0° C., and treated dropwise with thionyl chloride (0.122 mL, 1.68 mmol). The reaction mixture was allowed to warm to ambient temperature and was stirred for 3 h. The mixture was evaporated in vacuo to afford the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-93a8637e338f41ae968378ed3660ec92
Source noteuspto-grants-2011_10