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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474629Generated: October 30, 2026

Thionyl Chloride → 4-(Chloromethyl)-2-(trifluoromethyl)-1-{[3-(trifluoromethyl)phenyl]oxy}benzene

https://huagongshe.com/reaction/474629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(3-(Trifluoromethyl)-4-(3-(trifluoromethyl)phenoxy)phenyl)methanolHCID 86666206—
SolventDichloromethaneHCID 6344—
Product4-(Chloromethyl)-2-(trifluoromethyl)-1-{[3-(trifluoromethyl)phenyl]oxy}benzeneHCID 86666207109%

Reaction Steps

To a suspension of (3-(trifluoromethyl)-4-{[3-(trifluoromethyl)phenyl]oxy}phenyl) methanol (300 mg, 0.892 mmol) in DCM (4 mL) was added thionyl chloride (0.130 mL, 1.784 mmol) dropwise under nitrogen. The mixture was stirred at room temperature for 2 h. The mixture was stirred at room temperature for 2 h. The reaction was quenched with water, adjusted pH about 7 and extracted with DCM. The organic layer was separated and concentrated to afford the crude title compound (430 mg, 0.970 mmol, 109% yield) which can be used in next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-ebe4c44b815c4695a1571c3e1941c028
Source noteuspto-grants-2014_01