Reacción #61483

ord-d36d0a924f1d4a71acc735d20c1b7ca8

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato cool
  2. 2
    Filtraciónfiltered
  3. 3
    Extracciónthe filtrate extracted with ethyl acetate
  4. 4
    LavadoThe combined organic layers were washed with saturated sodium bicarbonate solution
  5. 5
    Otrodried
  6. 6
    Otroevaporated

Procedimiento

3-Trifluoracetyl-7-cyano-2,3,4,5-tetrahydro-1H-3-benzazepine (20.3 g) and nickel-aluminium alloy (35.5 g) in 75% aq. formic acid (400 ml) were heated at 80° C. for 3 h. The reaction was allowed to cool, filtered and the filtrate extracted with ethyl acetate. The combined organic layers were washed with saturated sodium bicarbonate solution, dried and evaporated to give 3-trifluoracetyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7-carbaldehyde (20.0 g) as a yellow oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07429579B2uspto-grants-2008_09