[3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanol → 3,5-Bis(dimethylamino)-4-(piperidin-1-yl)benzaldehyde
反応式
[CH3:1][N:2]([CH3:20])[C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([N:17]([CH3:19])[CH3:18])[C:10]=1[N:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)[CH2:6][OH:7]>[O-2].[O-2].[Mn+4].C(Cl)(Cl)Cl>[CH3:1][N:2]([CH3:20])[C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([N:17]([CH3:19])[CH3:18])[C:10]=1[N:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)[CH:6]=[O:7]参加物
4
実験手順
12.9 G. of 3,5-bis(dimethylamino)-4-piperidinobenzyl alcohol, 17.1 g. of activated manganese dioxide and 80 ml. of chloroform were mixed together and stirred at room temperature for 48 hours. The manganese dioxide was filtered off, washed with chloroform and the chloroform evaporated. After purification over aluminum oxide with benzene and recrystallization from ethanol, there was obtained 3,5-bis(dimethylamino)-4-piperidinobenzaldehyde having a melting point of 114°-116° C.