Reaktion #3474

ord-4a94e879ce5b4777a46e8ccc576b08e1

Reaktionsgleichung

COc1cccc2c1cc(C1CC1)n2Cc1ccccc1-c1ccccc1
1-([1,1'-biphenyl]-2-ylmethyl)-2-cyclopropyl-4-methoxyl-1H-indole
BrB(Br)Br
BBr3
ClCl
Cl2
Oc1cccc2c1cc(C1CC1)n2Cc1ccccc1-c1ccccc1
1-([1,1'-biphenyl]-2-ylmethyl)-2-cyclopropyl-4-hydroxy-1H-indole
Ausbeute 29.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe crude product was chromatographed on silica gel
  2. 2
    Wascheneluted with 20% EtOAc/hexane

Vorschrift

By the method used in Example 1, Part D, 1.25 g (3.7 mmol) of 1-([1,1'-biphenyl]-2-ylmethyl)-2-cyclopropyl-4-methoxyl-1H-indole was O-demethylated by treating it with 15 mL of 1M BBr3 /CH2 Cl2. The crude product was chromatographed on silica gel and eluted with 20% EtOAc/hexane to give 367 mg (29% yield) of 1-([1,1'-biphenyl]-2-ylmethyl)-2-cyclopropyl-4-hydroxy-1H-indole as an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733923uspto-grants-1998_03