Réaction #1747869

ord-d0d31b70ad7a4accb9f5af027c1b4417

Équation de réaction

O=C(Cl)c1ccc(I)cc1
4-iodobenzoyl chloride
Nc1ccccc1Nc1ccccc1
o-aminodiphenylamine
N
ammonia
Ic1ccc(-c2nc3ccccc3n2-c2ccccc2)cc1
N-Phenyl-2-(4-iodophenyl)benzimidazole

Solvants

Conditions de réaction

Température
75°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreformed from 85-90° C
  2. 2
    Autre(5 min)
  3. 3
    TempératureAfter cooling
  4. 4
    FiltrationThe precipitate was filtered off with suction
  5. 5
    Lavagewashed with ethanol
  6. 6
    workup.STIRRINGstirred up again in 400 ml of ethanol
  7. 7
    Autrewhich formed a solution which
  8. 8
    TempératureAfter cooling to 5-10° C.
  9. 9
    Filtrationthe precipitate was filtered off with suction
  10. 10
    Lavagewashed with cold ethanol
  11. 11
    Autredried at 75° C. in a vacuum
  12. 12
    Autredrying cabinet
  13. 13
    Autrewere obtained

Mode opératoire

37.47 g (136 mmol) of 97% 4-iodobenzoyl chloride and 12.82 g (68.2 mmol) of 98% o-aminodiphenylamine were heated to 100° C., in the course of which a stirrable melt formed from 85-90° C. Once the gas evolution had ended (5 min), the melt solidified. The reaction mixture was kept at 100° C. for another 3 hours. After cooling, it was admixed with 100 ml of ethanol with stirring. The precipitate was filtered off with suction, washed with ethanol and stirred up again in 400 ml of ethanol. The suspension was heated to 75° C., which formed a solution which was adjusted to pH 8 with 29 ml of 25% ammonia. After cooling to 5-10° C., the precipitate was filtered off with suction, washed with cold ethanol and dried at 75° C. in a vacuum drying cabinet. 18.37 g (68% of theory) of light gray microcrystals having an m.p. of 178-181° C. were obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08029919B2uspto-grants-2011_10