Reaktion #2419

ord-202ad24f23144e29a486e05cf3ccb4db

Reaktionsgleichung

CC(C)=O
acetone
O=S(=O)(O)O.O=S(=O)=O
oleum
NC(=O)c1cc(N)ccc1C(=O)Nc1ccc(N)cc1
4,4'-diamino-6-carbamoyl benzanilide
[NH4+].[OH-]
NH4OH
N#Cc1cc(N)ccc1C(=O)Nc1ccc(N)cc1
4,4'-diamino-6-cyanobenzanilide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturalready cooled down to -5° to 0° C
  2. 2
    WaschenThe solution was sufficiently washed
  3. 3
    Sonstigeto remove salt
  4. 4
    Filtrationby filtering
  5. 5
    Waschenwashed with a small amount of warm ethanol
  6. 6
    Sonstigedried in a vacuum oven at 80° C
  7. 7
    workup.ADDITIONThe dried reactant which was mixed with by-products
  8. 8
    Extraktionwas extracted by soxlet
  9. 9
    workup.ADDITIONtreated with the activated carbon
  10. 10
    workup.ADDITIONethanol was added
  11. 11
    Sonstigeto recrystallize in the mixture solvent (acetone:ethanol=1:1)
  12. 12
    FiltrationThe light yellow-scalelike crystal was filtered
  13. 13
    Sonstigedried in a vacuum oven at 80° C
  14. 14
    ExtraktionThe light yellow-scalelike crystal was extracted again by soxlet with acetone
  15. 15
    workup.ADDITIONtreated with the activated carbon
  16. 16
    SonstigeAnd then the white-scalelike crystal obtained
  17. 17
    Trocknenwas dried in a vacuum oven at 80° C. (40 g of the raw material
  18. 18
    Sonstigewas obtained
  19. 19
    Sonstigethereof was 250° to 251° C.

Vorschrift

350 ml of oleum (30% by weight) was cooled down below 0° C. using an ice bath, 99.6 g (0.368 mol) of 4,4'-diamino-6-carbamoyl benzanilide in a powder form was added below 5° C. with stirring. The stirring was continued to the next day, and the solution was neutralized by adding 1100 ml of NH4OH (28% by weight) already cooled down to -5° to 0° C. The solution was sufficiently washed to remove salt by filtering and washed with a small amount of warm ethanol and then dried in a vacuum oven at 80° C. The dried reactant which was mixed with by-products was extracted by soxlet and treated with the activated carbon and then ethanol was added to recrystallize in the mixture solvent (acetone:ethanol=1:1). The light yellow-scalelike crystal was filtered and dried in a vacuum oven at 80° C. The light yellow-scalelike crystal was extracted again by soxlet with acetone and treated with the activated carbon. And then the white-scalelike crystal obtained by recrystalling in the mixture solvent (acetone:ethanol=1:1) was dried in a vacuum oven at 80° C. (40 g of the raw material was obtained and the boiling point thereof was 250° to 251° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728799uspto-grants-1998_03