Reacción #47826
ord-87633b90324c42a59e3bb02d07e2d09b
Ecuación de reacción
Reactivos
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Filtraciónfiltered
- 2OtroThe organic layer was separated
- 3Concentraciónconcentrated under a reduced pressure
- 4OtroThe resulting residue was purified by flash chromatography
Procedimiento
1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (30 mg, 0.09 mmol) obtained in Example 18 was dissolved in ethanol (3 mL), silver nitrate (15.50 mg, 0.09 mmol) was added thereto, stirred for 3.5 hrs at RT, and filtered. The organic layer was separated, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 16 mg of the titled compound (yield: 52%).