Reacción #47817

ord-3c1bf3a9f67045bab896a8932ac5a56e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 24 hrs
  2. 2
    LavadoThe resulting mixture washed with sodium bicarbonate
  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
    OtroThen, the resulting residue was purified by flash chromatography

Procedimiento

1-Oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl ester (2 g, 4.85 mmol) obtained in Example 7 was dissolved in methanol, p-toluenesulfonic acid (92 mg, 0.49 mmol) was added thereto, and refluxed for 24 hrs. The resulting mixture washed with sodium bicarbonate and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. Then, the resulting residue was purified by flash chromatography to obtain 1.2 g of the titled compound (yield: 62%).

Fuente

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