Reaktion #1463481
ord-a4ab46ba8619492eb98683363652c4eb
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeInto a three-necked flask equipped with a dropping funnel
- 2Sonstigereached 10° C
- 3SonstigeThe resulting reaction mixture
- 4Sonstigeup to room temperature
- 5Sonstigefor one hour
- 6workup.STIRRINGstirring for one hour
- 7workup.STIRRINGfurther stirring the reaction mixture for 5 hours
- 8workup.ADDITIONafter completion of the dropwise addition
- 9Filtrationfiltering off
- 10Einengenconcentrating the filtrate under reduced pressure
- 11Sonstigeisolating
- 12Sonstigepurifying the resulting pale brown oil by means of silica gel column chromatography
Vorschrift
Into a three-necked flask equipped with a dropping funnel, a three-way cook and a thermometer was placed 2-(1,3-dioxan-2-yl)ethyltriphenylphosphonium bromide (9.1 g, 20 mmols), followed by adding tetrahydrofuran (100 ml), suspending, stirring under ice cooling till the liquid temperature reached 10° C. The resulting reaction mixture was added potassium t-butoxide (2.2 g, 20 mmols) followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (50 ml) solution of 4-(3-fluoro-4-trifluoromethoxyphenyl)cyclohexanone (5.5 g, 20 mmols) over 30 minutes from the dropping funnel, further stirring the reaction mixture for 5 hours after completion of the dropwise addition, adding ether (100 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure, and isolating and purifying the resulting pale brown oil by means of silica gel column chromatography, to obtain 1-(2-(1,3-dioxan-2-yl)ethylidene)-4-(3-fluoro-4-trifluoromethoxyphenyl)cyclohexane.