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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Difluorobenzonitrile | HCID 587204 | — |
| Reactant | HCID 178516505 | HCID 178516505 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | 3,5-Bis-(2-trifluoromethylpyridin-4-yloxy)benzonitrile | HCID 11560919 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750222B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-8bd2a47560894c11a47af83b98b5e951 |
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| Source note | uspto-grants-2004_06 |
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