Reaktion #483760

ord-7b85a55b0cb4490eb393b2b409b3a59b

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 is washed with brine
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Einengenconcentrated at reduced pressure
  6. 6
    SonstigeThe residue is chromatographed on silica gel
  7. 7
    Wascheneluted with 20% EtOAc/hexane

Vorschrift

2-Ethyl-4-methoxy-1H-indole (4.2 g, 24 mmol) is dissolved in 30 mL of DMF and 960 mg (24 mmol) of 60% NaH/minerial oil is added. After 1.5 hours, 2.9 mL(24 mmol) of benzyl bromide is added. After 4 hours, the mixture is diluted with water and extracted twice with ethyl acetate. The combined ethyl acetate is washed with brine, dried (MgSO4) and concentrated at reduced pressure. The residue is 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: US06608099B1uspto-grants-2003_08