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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942972Generated: October 31, 2026

Cesium carbonate → 4-(Trifluoromethyl)-2-(6-(trifluoromethyl)pyridin-3-yloxy)benzonitrile

https://huagongshe.com/reaction/1942972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Fluoro-4-(trifluoromethyl)benzonitrileHCID 518973—
Reactant5-Hydroxy-2-(trifluoromethyl)pyridineHCID 2783388—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Trifluoromethyl)-2-(6-(trifluoromethyl)pyridin-3-yloxy)benzonitrileHCID 5768770987.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-fluoro-4-(trifluoromethyl)benzonitrile (0.19 g, 1.0 mmol), 6-(trifluoromethyl)pyridin-3-ol (0.16 g, 1.0 mmol), and Cs2CO3 (0.33 g, 1 mmol) in DMF (10 mL) was stirred at 60° C. for 18 hours. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were washed with brine and water, dried over sodium sulfate, and evaporated. The residue was purified by column chromatography on silica gel with 0-15% ethyl acetate in hexanes to give 4-(trifluoromethyl)-2-(6-(trifluoromethyl)pyridin-3-yloxy)benzonitrile (0.29 g, 87% yield). LC/MS: m/z 333.5 (M+H)+ at 1.83 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389734B2
Source datasetuspto-grants-2013_03
ORD IDord-b808250918dc440695f3f854f6993bb9
Source noteuspto-grants-2013_03