Réaction #6955

ord-183102cc420b4877ac00ee09af6bc6a9

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreTo 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
    AutreThe reaction mixture was partitioned between ethyl acetate and brine
  5. 5
    Séchagethe organic phase dried with MgSO4
  6. 6
    Autrethe solvent was removed under reduced pressure
  7. 7
    AutreThe crude product was purified by silica gel chromatography

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07084159B2uspto-grants-2006_08