Reaktion #2486785
ord-dab7877a10834ae7ab881274c23aeb33
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeInto a three-necked flask equipped with a dropping funnel
- 2Sonstigereached 10° C
- 3Sonstigeup to room temperature
- 4Sonstigefor one hour
- 5workup.STIRRINGstirring for one hour
- 6workup.STIRRINGfurther stirring the reaction mixture for 5 hours
- 7workup.ADDITIONafter completion of the dropwise addition
- 8Filtrationfiltering off
- 9Einengenconcentrating the filtrate under reduced pressure
- 10Sonstigeisolating
- 11Sonstigepurifying the resulting pale brown oily substance by means of silica gel column chromatography
- 12Sonstigerecrystallizing from ethanol
Vorschrift
Into a three-necked flask equipped with a dropping funnel, a three-way cock and a thermometer was placed (2-(1,3-dioxan)-2-yl)ethyl)triphenylphosphonium bromide (12.3 g, 27 mmols), followed by adding tetrahydrofuran (50 ml), suspending, stirring under ice cooling till the liquid temperature reached 10° C. The reaction mixture is added potassium t-butoxide (3.0 g, 27 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (10 ml) solution of 4-(4-propylcyclohexyl)cyclohexanone (15.6 g, 25 mols) over 30 minutes from the dropping funnel, further stirring the reaction mixture for 5 hours after completion of the dropwise addition, adding ether (50 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure, isolating and purifying the resulting pale brown oily substance by means of silica gel column chromatography and recrystallizing from ethanol, to obtain 1-(2-(1,3-dioxan)-2-yl)ethylidene)-4-(4-propylcyclohexyl)cyclohexane (4.5 g, 14 mmols).