Reacción #46174
ord-3b200dad4b06471d9b74686d147c1eb5
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe mixture was reacted for 1 hour at 70° C.
- 2Lavadowashed with brine
- 3ExtracciónThe organic layer was extracted with ethyl acetate
- 4Secadodried over anhydrous sulfonate sulfate
- 5Concentraciónconcentrated
- 6Otrothe 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.