Reacción #54657

ord-b08268a4f0fc4ef6a5dfe4c006fb152a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas hydrogenated at room temperature in 945 ml
  2. 2
    FiltraciónThe catalyst was filtered
  3. 3
    Otrothe filtrate was evaporated in vacuo to a solid residue
  4. 4
    OtroThe residue was chromatographed over silica gel
  5. 5
    Otroto yield 43.6 g

Procedimiento

Fifty grams of 4-amino-3-nitrobenzophenone was hydrogenated at room temperature in 945 ml. of tetrahydrofuran with 15 g. of Raney nickel at 40 psi. After 4 hours three equivalents of hydrogen were absorbed. The catalyst was filtered and the filtrate was evaporated in vacuo to a solid residue. The residue was chromatographed over silica gel using ethyl acetate as eluant. Fractions 5-9 were combined to yield 43.6 g. (100 percent yield) of 3,4-diaminobenzophenone.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04150028uspto-grants-1979_04