Réaction #1243

ord-d0e79d3004cd4cb5a98d3c999a726a05

Équation de réaction

N#CCc1ccc(F)cc1
4-fluorophenyl-acetonitrile
[Na+].[OH-]
sodium hydroxide
O=[N+]([O-])c1ccccc1
nitrobenzene
Fc1ccc(-c2onc3ccccc23)cc1
3-(4-fluorophenyl)-2,1-benzisoxazole

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe resulting solution is warmed to 65°-70° C.
  2. 2
    Températurecooled in an ice bath
  3. 3
    FiltrationThe resulting dark precipitate is filtered
  4. 4
    Lavagewashed with cold methanol until the methanol washings
  5. 5
    AutreThe product (16) is recrystallized from toluene

Mode opératoire

A total of 50.7 g (0.375 mol) of 4-fluorophenyl-acetonitrile is slowly added to a vigorously stirred, room-temperature solution of 150 g (3.75 mol) of sodium hydroxide in 750 ml of absolute methanol. After solution is complete, 46 g (0.374 mol) of nitrobenzene is slowly added. The resulting solution is warmed to 65°-70° C. and held at this temperature for 9 hours. The dark slurry is cooled to room temperature, diluted with 250 ml of 50% methanol, and cooled in an ice bath. The resulting dark precipitate is filtered and washed with cold methanol until the methanol washings were clear. The product (16) is recrystallized from toluene.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723573uspto-grants-1998_03