HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762258Generated: November 2, 2026
Cesium fluoride → 2,3-Difluoro-5-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/1762258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Chloro-3-fluoro-5-(trifluoromethyl)pyridine | HCID 12919753 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | 2,3-Difluoro-5-(trifluoromethyl)pyridine | HCID 13421547 | 91% |
Reaction Steps
47.7 g (0.82 mol) of potassium fluoride and 10.0 g (0.065 mol) of caesium fluoride are suspended in 300 ml of sulfolane and the suspension is heated to 140° C. 60 ml of sulfolane are distilled off by decreasing the pressure and subsequently 65.6 g (0.329 mol) of 2-chloro-3-fluoro-5-trifluoromethylpyridine and 1.3 g (0.004 mol) of 18-crown-6 are added. The reaction mixture is stirred for 48 hours at 140° C. and subsequently distilled by introducing steam. The oil is separated and the aqueous phase is extracted twice with a small amount of ether. The organic phases are purified, dried with a small amount of magnesium sulfate and filtered. Distillation affords 54.8 g (91% of theory) of 2,3-difluoro-5-trifluoromethylpyridine, b.p. 100°-102° C. (980 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831148 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-923ff52ecd2149ccb3892b9580af52fe |
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| Source note | uspto-grants-1989_05 |
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