Reacción #1463482
ord-41fc16c337c24790b26ea80cc98d22e4
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroInto a three-necked flask equipped with a dropping funnel
- 2Otroreached 10° C
- 3OtroThe resulting reaction mixture
- 4Otroup to room temperature
- 5Otrofor one hour
- 6workup.STIRRINGstirring for one hour
- 7workup.STIRRINGfurther stirring
- 8Otrothe reaction liquid for 5 hours
- 9workup.ADDITIONafter completion of the dropwise addition
- 10Filtraciónfiltering off
- 11Concentraciónconcentrating the filtrate under reduced pressure
- 12Otroisolating
- 13Otropurifying the resulting pale brown oil by means of silica gel column chromatography
Procedimiento
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)ethyltriphenylphosphonium bromide (22.9 g, 50 mmols), followed by adding tetrahydrofuran (100 ml), suspending, stirring the suspension under ice cooling till the liquid temperautre reached 10° C. The resulting reaction mixture is added potassium t-butoxide (5.6 g, 50 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (100 ml) solution of (4-(4-propylphenyl)phenyl)cyclohexanone (14.0 g, 48 mmols) over 30 minutes from the dropping funnel, further stirring the reaction liquid for 5 hours after completion of the dropwise addition, adding ether (200 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-(4-(4-propylphenyl)phenylcyclohexane.