Reacción #3458

ord-e34bd1862e53447ea8a43dbc7cad8a0e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter 4 hours
  2. 2
    Extracciónextracted twice with ethyl acetate
  3. 3
    LavadoThe combined ethyl acetate was washed with brine
  4. 4
    Secadodried (MgSO4)
  5. 5
    Concentraciónconcentrated at reduced pressure
  6. 6
    OtroThe residue was chromatographed on silica gel
  7. 7
    Lavadoeluted with 20% EtOAc/hexane

Procedimiento

2-Ethyl-4-methoxy-1H-indole (4.2 g, 24 mmol) was dissolved in 30 mL of DMF and 960 mg (24 mmol) of 60% NaH/mineral oil was added. After 1.5 hours, 2.9 mL (24 mmol) of benzyl bromide was added. After 4 hours, the mixture was diluted with water and extracted twice with ethyl acetate. The combined ethyl acetate was washed with brine, dried (MgSO4) and concentrated at reduced pressure. The residue was chromatographed on silica gel and eluted with 20% EtOAc/hexane to give 3.1 g (49% yield) of 2-ethyl-4-methoxy-1-(phenylmethyl)-1H-indole.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733923uspto-grants-1998_03