Reaktion #668603

ord-2d1b3c206ad84fa8a4875c64839042e9

Reaktionsgleichung

CCc1cc2c(OC)cccc2[nH]1
2-Ethyl-4-methoxy-1H-indole
[H-].[Na+]
NaH
BrCc1ccccc1
benzyl bromide
CCc1cc2c(OC)cccc2n1Cc1ccccc1
2-ethyl-4-methoxy-1-(phenylmethyl)-1H-indole
Ausbeute 49.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITAfter 4 hours
  2. 2
    Extraktionextracted twice with ethyl acetate
  3. 3
    WaschenThe combined ethyl acetate was washed with brine
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Einengenconcentrated at reduced pressure
  6. 6
    SonstigeThe residue was chromatographed on silica gel
  7. 7
    Wascheneluted with 20% EtOAc/hexane

Vorschrift

2-Ethyl-4-methoxy-1H-indole (4.2 g, 24 mmol) was dissolved in 30 mL of DMF and 960mg (24 mol) 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05919943uspto-grants-1999_07