Reacción #47826

ord-87633b90324c42a59e3bb02d07e2d09b

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónfiltered
  2. 2
    OtroThe organic layer was separated
  3. 3
    Concentraciónconcentrated under a reduced pressure
  4. 4
    OtroThe 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%).

Fuente

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