Réaction #531813
ord-7828509d36134cdb89b22cfb65774069
Équation de réaction
2,3-dichloropyridine
3-(trifluoromethyl)-pyrazole
potassium carbonate
→
desired intermediate
Rendement 75.1%
3-chloro-2-[3-(trifluoromethyl)-1H-pyrazol-1-yl]pyridine
Rendement 75.1%
Réactifs
Aucun
Solvants
Conditions de réaction
Température
117.5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1TempératureThe reaction was cooled to 100° C.
- 2Filtrationfiltered through Celite® diatomaceous filter aid
- 3Autreto remove solids
- 4AutreN,N-Dimethylformamide and excess dichloropyridine were removed by distillation at atmospheric pressure
- 5workup.DISTILLATIONDistillation of the product at reduced pressure (b.p. 139-141° C., 7 mm)
Mode opératoire
To a mixture of 2,3-dichloropyridine (99.0 g, 0.67 mol) and 3-(trifluoromethyl)-pyrazole (83 g, 0.61 mol) in dry N,N-dimethylformamide (300 mL) was added potassium carbonate (166.0 g, 1.2 mol) and the reaction was then heated to 110-125° C. over 48 hours. The reaction was cooled to 100° C. and filtered through Celite® diatomaceous filter aid to remove solids. N,N-Dimethylformamide and excess dichloropyridine were removed by distillation at atmospheric pressure. Distillation of the product at reduced pressure (b.p. 139-141° C., 7 mm) afforded 113.4 g of the desired intermediate as a clear yellow oil.