Reacción #565372

ord-29d6a6c76aba42dd88801346e36fbcae

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroTo the resulting reaction mixture
  2. 2
    workup.STIRRINGthe reaction mixture stirred at ambient temperature for 3 hours
  3. 3
    workup.STIRRINGthe resulting mixture was stirred at ambient temperature overnight
  4. 4
    OtroThe reaction mixture was partitioned between ethyl acetate and brine
  5. 5
    Secadothe organic phase dried with MgSO4
  6. 6
    Otrothe solvent was removed under reduced pressure
  7. 7
    OtroThe crude product was purified by silica gel chromatography

Procedimiento

To a solution of 3-cyclohexyl-3-oxo-propionitrile in DMF:CS2 (1:1) was added K2CO3 at 0° C. and the reaction mixture stirred at ambient temperature for 2 hours. To the resulting reaction mixture was added chloroacetone (1 equivalent) and the reaction mixture stirred at ambient temperature for 3 hours. Iodomethane was then added and the resulting mixture was stirred at ambient temperature overnight. The reaction mixture was partitioned between ethyl acetate and brine, the organic phase dried with MgSO4 and the solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06642227B2uspto-grants-2003_11