Reacción #54340

ord-527562608acf4740b940b721b5a2be8e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe reaction mixture is filtered through diatomaceous earth with ethyl acetate
  2. 2
    Otroevaporated
  3. 3
    OtroThe residue is recrystallized from ethyl acetate
  4. 4
    Otroto yield 3.8 g

Procedimiento

A mixture of 8.5 (17.03 mmols) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-3-hydroxypiperidine, 2.0 g. of 10% palladium-on-carbon and 60 ml. of ethanol is stirred under one atmosphere of hydrogen for 2 hours. The reaction mixture is filtered through diatomaceous earth with ethyl acetate and evaporated. The residue is recrystallized from ethyl acetate to yield 3.8 g. (70%) of the title compound. A second crop of the title compound 0.396 g. (7%) is obtained from the mother liquor.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04147872uspto-grants-1979_04