Reaktion #47826

ord-87633b90324c42a59e3bb02d07e2d09b

Reaktionsgleichung

CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester
CCO
ethanol
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OCC
titled compound
Ausbeute 52.0%
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OCC
1-ethoxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic Acid Ethyl Ester
Ausbeute 52.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered
  2. 2
    SonstigeThe organic layer was separated
  3. 3
    Einengenconcentrated under a reduced pressure
  4. 4
    SonstigeThe resulting residue was purified by flash chromatography

Vorschrift

1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (30 mg, 0.09 mmol) obtained in Example 18 was dissolved in ethanol (3 mL), silver nitrate (15.50 mg, 0.09 mmol) was added thereto, stirred for 3.5 hrs at RT, and filtered. The organic layer was separated, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 16 mg of the titled compound (yield: 52%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745439B2uspto-grants-2010_06