Reacción #47818

ord-da7fdcea465a4d1482f088d4455d5142

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroUpon the completion of the reaction
  2. 2
    Lavadothe mixture washed with saturated saline
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    OtroThe organic layer was separated
  5. 5
    Secadodried over anhydrous MgSO4
  6. 6
    Concentraciónconcentrated under a reduced pressure
  7. 7
    OtroThe resulting residue was purified by flash chromatography

Procedimiento

1-Oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carbonitrile (350 mg, 0.878 mmol) obtained in Step 1 was dissolved in THF, and phenylmagnesium chloride (0.483 mL, 0.966 mmol) was added thereto, followed by stirring for 3 hrs at 0° C. Upon the completion of the reaction, the mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 378 mg of the titled compound (yield: 90%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745439B2uspto-grants-2010_06