Reaktion #46154
ord-9f1d80b364074f929dd880780932bf51
Reaktionsgleichung
1-Bromo-3-phenylpropane
6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester
potassium carbonate
sodium iodide
→
title compound
Ausbeute 85.0%
3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester
Ausbeute 85.0%
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Waschenwashed with saturated ammonium chloride
- 2SonstigeThe organic layer obtained
- 3Extraktionby extracting the reaction mixture with ethyl acetate
- 4Trocknenwas dried over anhydrous magnesium sulfate
- 5Einengenconcentrated
- 6Sonstigethe 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.