(4-Cyanobenzyl)triphenylphosphonium chloride → 4-[2-(p-Cyanophenyl)vinyl]cyclohexanone
反応式
[Cl-].[C:2]([C:4]1[CH:29]=[CH:28][C:7]([CH2:8][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:6][CH:5]=1)#[N:3].[CH:30]([CH:32]1[CH2:37][CH2:36][C:35](=[O:38])[CH2:34][CH2:33]1)=O>COCCOC>[C:2]([C:4]1[CH:5]=[CH:6][C:7]([CH:8]=[CH:30][CH:32]2[CH2:37][CH2:36][C:35](=[O:38])[CH2:34][CH2:33]2)=[CH:28][CH:29]=1)#[N:3]参加物
4
反応条件
- 温度
- 0 °C
実験手順
63.3 g of p-cyanobenzyl-triphenylphosphonium chloride, 17.2 g of potassium t-butylate and 195 ml of ethylene glycol dimethyl ether were placed in a sulphonation flask while stirring and gassing with nitrogen, whereby the internal temperature rose to 44° C. The brown suspension was cooled to 0° C. and treated within 2 minutes with a solution of 16.7 g of 4-formylcyclohexanone in 100 ml of ethylene glycol dimethyl ether. Thereafter, the cooling bath was removed and the reaction mixture was stirred for a further 3.5 hours at room temperature. The suspension was subsequently poured into 500 ml of water and extracted three times with 600 ml of methylene chloride each time. The organic phases were washed twice with 500 ml of 10% (wt./vol.) sodium chloride solution each time, dried over sodium sulphate, filtered and concentrated, whereby 76.9 g of a brownish paste remained behind. Chromatographic separation of this crude product on silica gel with methylene chloride as the eluent gave 33.0 g of 4-[ 2-(p-cyanophenyl)vinyl]cyclohexanone as a yellow-brownish oil.