Réaction #40715
ord-0253a7c0b59e4adb8b82bec7322589c9
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Autrewere at 0-5° C.
- 2workup.ADDITIONwas added dropwise
- 3AutreThe mixture was subsequently quenched with ice-water
- 4workup.ADDITIONby adding NaOH
- 5FiltrationThe resulting solid was filtered off
- 6Extractionthe solution was extracted with dichloromethane
- 7Autrethe organic phase was dried
- 8Concentrationconcentrated
- 9AutreThe oil obtained in this way
- 10Températurethe reaction mixture was heated at 55° C. for 3 hours
- 11Autrethe solvent was evaporated
- 12Autredried
Mode opératoire
11.08 ml of N,N-dimethylformamide was slowly added dropwise to 11.03 ml of POCl3 were at 0-5° C. while stirring and, after about 5 minutes a solution of 2-fluorophenylacetic acid (6 g, 38.9 mmol) in 20 ml of N,N-dimethylformamide was added dropwise. The mixture was then heated at 70° C. for about 17 hours. The mixture was subsequently quenched with ice-water and the mixture was made alkaline by adding NaOH. The resulting solid was filtered off, the solution was extracted with dichloromethane, and the organic phase was dried and concentrated. The oil obtained in this way was directly dissolved in 50 ml of ethanol. 7.3 ml of hydrazine hydrate were added, and the reaction mixture was heated at 55° C. for 3 hours. After the reaction was complete, the solvent was evaporated and the remaining solid was stirred with water and then dried. 2.65 g of 4-(2-fluorophenyl)-1H-pyrazole were obtained.