Reaktion #46154

ord-9f1d80b364074f929dd880780932bf51

Reaktionsgleichung

BrCCCc1ccccc1
1-Bromo-3-phenylpropane
CCOC(=O)C1=C(c2ccccc2)c2ccc(O)cc2C1=O
6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[Na+]
sodium iodide
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
title compound
Ausbeute 85.0%
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester
Ausbeute 85.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with saturated ammonium chloride
  2. 2
    SonstigeThe organic layer obtained
  3. 3
    Extraktionby extracting the reaction mixture with ethyl acetate
  4. 4
    Trocknenwas dried over anhydrous magnesium sulfate
  5. 5
    Einengenconcentrated
  6. 6
    Sonstigethe residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4)

Vorschrift

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (2 g, 6.80 mmol), potassium carbonate (1.41 g, 10.194 mmol), and sodium iodide (200 mg, 1.359 mmol) were dissolved in dimethylformamide (100 ml). 1-Bromo-3-phenylpropane (2.01 ml, 13.59 mmol) was added thereto at room temperature, was stirred for 12 hours at 60° C., and washed with saturated ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4) to obtain the title compound (yield 85%) as a dark red solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741323B2uspto-grants-2010_06