Reacción #82741

ord-5fefe3598c414c188fafb39f98450eee

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat room temperature
  2. 2
    Filtraciónthe mixture was filtered through a bed of celite
  3. 3
    Concentraciónthe filtrate concentrated in vacuo
  4. 4
    Otroto give
  5. 5
    workup.ADDITIONa mixture of a solid which
  6. 6
    Otrothe product recrystallized from a mixture of cyclohexane:ethyl acetate (3:1)

Procedimiento

40 gms (Aldrich lot #CY 02301 HX, containing 15% of the 3-nitro isomer) of 5-nitroacenaphthene was dissolved in a mixture of tetrahydrofuran (150 ml) and acetic acid (25 ml.). To this solution was added 1.0 of 10% Pd/C and the mixture hydrogenated (40 psi) at room temperature. After 2 hours, the mixture was filtered through a bed of celite and the filtrate concentrated in vacuo to give a mixture of a solid which darkened (to purple) considerably on exposure to air. This material was redissolved in methylene chloride and decolorized with activated charcoal and then the product recrystallized from a mixture of cyclohexane:ethyl acetate (3:1) to give 8.3 g of clean material--only the major 5-amino isomer being present by TLC. This material was used as is directly in the next step.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05622968uspto-grants-1997_04