Reaktion #1500881
ord-52b76aefbe504e29bea110c623960527
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigewas prepared
- 2TemperaturThe reaction mixture was heated
- 3Temperaturto reflux for 1 hour
- 4Temperaturcooled to 0°
- 5TemperaturAfter cooling the reaction mixture at -8°
- 6Extraktionwas extracted with ether (3×300 ml)
- 7Waschenwashed with water (3×100 ml)
- 8Trocknendried over sodium sulfate
- 9Sonstigefinally evaporated
- 10Sonstigeto afford 13.2 g of raw material
- 11SonstigeAfter purification
- 12workup.DISTILLATIONby means of column chromatography (neutral Al2O3 --eluent:toluene) and subsequent distillation on a VIGREUX column
Vorschrift
3-Cyclohexyl-cyclopentanone used hereinabove as starting material was prepared as indicated hereinafter: 16.6 g (0.148 Mole) of cyclohexyl chloride were added dropwise to 3.6 g (0.150 atome-g) of magnesium metal in a 250 ml vessel, under nitrogen atmosphere and in the presence of a iodine cristal. The reaction mixture was heated to reflux for 1 hour, then cooled to 0° and 1.42 g (0.074 Mole) of cuprous iodide were added thereto. After cooling the reaction mixture at -8°, 5.74 g (0.070 Mole) of cyclopent-2-ene-1-one in 40 ml of tetrahydrofurane were added dropwise. After having been stirred for 1 hour at -8°, the reaction mixture was poured onto 100 g of crushed ice, acidified with 15% HCl in water (pH 4-5) and finally neutralized by the addition of aqueous ammonia. After the addition of 10 g of NH4Cl the reaction mixture was extracted with ether (3×300 ml), washed with water (3×100 ml), dried over sodium sulfate and finally evaporated to afford 13.2 g of raw material. After purification by means of column chromatography (neutral Al2O3 --eluent:toluene) and subsequent distillation on a VIGREUX column, there were obtained 7.0 g (60% yield) of the desired product, b.p. 50°/0.005 Torr.