Reacción #47825
ord-1046f77f00fd4ad4b67f07f851c18159
Ecuación de reacción
Reactantes
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 (60 mg, 0.18 mmol) obtained in Step 1 was dissolved in methanol (10 mL), silver nitrate (37.20 mg, 0.22 mmol) was added thereto, stirred for 3 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 14 mg of the titled compound (yield: 24%).