反応 #1463482
ord-41fc16c337c24790b26ea80cc98d22e4
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1その他Into a three-necked flask equipped with a dropping funnel
- 2その他reached 10° C
- 3その他The resulting reaction mixture
- 4その他up to room temperature
- 5その他for one hour
- 6workup.STIRRINGstirring for one hour
- 7workup.STIRRINGfurther stirring
- 8その他the reaction liquid for 5 hours
- 9workup.ADDITIONafter completion of the dropwise addition
- 10ろ過filtering off
- 11濃縮concentrating the filtrate under reduced pressure
- 12その他isolating
- 13その他purifying the resulting pale brown oil by means of silica gel column chromatography
実験手順
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.