Réaction #40715

ord-0253a7c0b59e4adb8b82bec7322589c9

Solvants

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrewere at 0-5° C.
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    AutreThe mixture was subsequently quenched with ice-water
  4. 4
    workup.ADDITIONby adding NaOH
  5. 5
    FiltrationThe resulting solid was filtered off
  6. 6
    Extractionthe solution was extracted with dichloromethane
  7. 7
    Autrethe organic phase was dried
  8. 8
    Concentrationconcentrated
  9. 9
    AutreThe oil obtained in this way
  10. 10
    Températurethe reaction mixture was heated at 55° C. for 3 hours
  11. 11
    Autrethe solvent was evaporated
  12. 12
    Autredried

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07728012B2uspto-grants-2010_06