Reacción #6913

ord-50a401181684469192a5170e3a2ba065

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroPrepared
  2. 2
    Temperaturawarmed
  3. 3
    Temperaturato reflux under N2
  4. 4
    Temperaturaat reflux
  5. 5
    TemperaturaAfter cooling
  6. 6
    Otrothe reaction to rt
  7. 7
    OtroThe volatiles were removed
  8. 8
    workup.ADDITIONfrexh methanol was added to the resulting residue
  9. 9
    OtroAgain, the volatiles were removed
  10. 10
    Lavadowashed with saturated potassium carbonate (aqueous)
  11. 11
    SecadoThe organic layer was dried over sodium sulfate
  12. 12
    Otrothe volatiles were removed

Procedimiento

Prepared according to Procedure K. 2-iso-Propylsulfonylacetonitrile (0.50 g, 3.39 mmol) was dissolved in THF and warmed to reflux under N2. Borane dimethylsulfide (2M, 1.7 mL, 3.39 mmol) was added dropwise and the reaction was stirred for an additional 40 minutes at reflux. After cooling the reaction to rt, HCl (2 M in MeOH) was added to the reaction slowly due to gas evolution. The volatiles were removed and frexh methanol was added to the resulting residue. Again, the volatiles were removed and the resulting residue was taken up in CH2Cl2 (25 mL) and washed with saturated potassium carbonate (aqueous). The organic layer was dried over sodium sulfate and the volatiles were removed to afford the title compound. GC-MS m/z 152 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084147B2uspto-grants-2006_08