Reacción #46174

ord-3b200dad4b06471d9b74686d147c1eb5

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe mixture was reacted for 1 hour at 70° C.
  2. 2
    Lavadowashed with brine
  3. 3
    ExtracciónThe organic layer was extracted with ethyl acetate
  4. 4
    Secadodried over anhydrous sulfonate sulfate
  5. 5
    Concentraciónconcentrated
  6. 6
    Otrothe resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9)

Procedimiento

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester (1.65 g, 4.0 mmol) prepared in (Step 5) of Example 1 was dissolved in methanol (160 ml) and p-toluene sulfonic acid (228 mg, 1.2 mmol) was added thereto. The mixture was reacted for 1 hour at 70° C., and then washed with brine. The organic layer was extracted with ethyl acetate, dried over anhydrous sulfonate sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9) to obtain the title compound (yield 75.3%) as a red solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741323B2uspto-grants-2010_06