Reaction #792155
ord-7d10b2a860144bb8bee62a2d7ec7ef7c
Reaction equation
2,3-dichloropyridine
3-(trifluoromethyl)-pyrazole
potassium carbonate
→
desired intermediate
Yield 75.1%
3-Chloro-2-[3-(trifluoromethyl)-1H-pyrazol-1-yl]pyridine
Yield 75.1%
Reagents
None
Solvents
Conditions
Temperature
117.5°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1TemperatureThe reaction was cooled to 100° C.
- 2Filtrationfiltered through Celite® diatomaceous filter aid
- 3Otherto remove solids
- 4OtherN,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)
Procedure
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 the desired intermediate as a clear yellow oil (113.4 g).