Reacción #95103

ord-2380d4f359754994b05163591b874988

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter evaporation
  2. 2
    Otrothe residue obtained
  3. 3
    Otrowas chromatographed on silicagel (solvent: toluene/acetone (20.1))

Procedimiento

An amount of 23.5 g (63.3 m mole) of 5-benzyloxy-3-phenyl-1H-2-indole-carboxylic acid ethylester in absolute dimethylformamide was mixed with 3.0 g (63.3 m mole) of 50% sodium hydride. After 30 minutes, 13.2 g (63.3 m mole) of 5-bromo-valeric acid ethylester were added, and the mixture was stirred for three days. After evaporation, the residue obtained was chromatographed on silicagel (solvent: toluene/acetone (20.1)).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04343811uspto-grants-1982_08