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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353205Generated: October 30, 2026

Water → 3,5-Bis-(2-trifluoromethylpyridin-4-yloxy)benzonitrile

https://huagongshe.com/reaction/353205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-DifluorobenzonitrileHCID 587204—
ReactantHCID 178516505HCID 178516505—
SolventDimethylacetamideHCID 31374—
SolventEthylacetate heptaneHCID 21899848—
Product3,5-Bis-(2-trifluoromethylpyridin-4-yloxy)benzonitrileHCID 11560919—

Reaction Conditions

Temperature150 °C

Reaction Steps

Under an atmosphere of nitrogen, 0.556 g (4.0 mmol) of 3,5-difluorobenzonitrile was initially charged in 10 ml of N,N-dimethylacetamide, and 1.22 g (8.8 mmol) of potassium carbonate were added a little at a time at room temperature. 1.305 g (8.00 mmol) of 2-(trifluoromethyl)pyridin-4-ol were then added and the mixture was heated at 150° C. for 30 h and cooled to room temperature, water and ethyl acetate/heptane (1:1) were added to the reaction solution and the solution was stirred for a number of minutes. The phases were separated and the organic phase was washed repeatedly with water and finally with saturated sodium chloride solution and then dried over sodium sulfate, filtered and concentrated. HPLC of the crude product gave 3,5-bis-(2-trifluoromethylpyridin-4-yloxy)benzonitrile in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750222B2
Source datasetuspto-grants-2004_06
ORD IDord-8bd2a47560894c11a47af83b98b5e951
Source noteuspto-grants-2004_06