Reaktion #439112

ord-aedfb14ae3144d6d8767b8e89bac1c8d

Reaktionsgleichung

CCOC(=O)CC(c1ccccc1)c1c[nH]c2cc(O)ccc12
ethyl 3-phenyl-3-(6-hydroxyindol-3-yl)propionate
CCOC(=O)CC(c1ccccc1)c1c[nH]c2cc(O)ccc12
Ethyl 3-phenyl-3-(6-hydroxyindol-3-yl)propionate
CC(C)(C)OC(=O)CBr
tert-butyl bromoacetate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=O.Cc1ccccc1
toluene acetone
CCOC(=O)CC(c1ccccc1)c1c[nH]c2cc(OCC(=O)OC(C)(C)C)ccc12
ethyl 3-phenyl-3-[6-(tert-butoxycarbonylmethoxy)indol-3-yl]propionate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe residue is filtered off
  2. 2
    Sonstigethe solution is evaporated
  3. 3
    Sonstigethe crude product is purified by chromatography on silica gel (eluent toluene/acetone 9:1)

Vorschrift

The compound ethyl 3-phenyl-3-(6-hydroxyindol-3-yl)propionate 4 prepared analogously to Example 1.1-1.3 (3.23 mmol) is stirred overnight at 60° C. with 0.94 ml (6.4 mmol) of tert-butyl bromoacetate and 1.8 g (13 mmol) of potassium carbonate in 20 ml of acetone. When the reaction is complete (TLC check toluene/acetone 4:1), the residue is filtered off, the solution is evaporated, and the crude product is purified by chromatography on silica gel (eluent toluene/acetone 9:1), giving ethyl 3-phenyl-3-[6-(tert-butoxycarbonylmethoxy)indol-3-yl]propionate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06743810B2uspto-grants-2004_06