Reaktion #47825

ord-1046f77f00fd4ad4b67f07f851c18159

Reaktionsgleichung

CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
1-bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic Acid Ethyl Ester
CO
methanol
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
titled compound
Ausbeute 24.0%
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
1,6-dimethoxy-3-phenyl-1H-indene-2-carboxylic Acid Ethyl Ester
Ausbeute 24.0%

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 (60 mg, 0.18 mmol) obtained in Step 1 was dissolved in methanol (10 mL), silver nitrate (37.20 mg, 0.22 mmol) was added thereto, stirred for 3 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 14 mg of the titled compound (yield: 24%).

Quelle

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