Triacetoxyperiodinane → 4-[5-(4-Isobutylphenyl)-1,3,4-oxadiazol-2-yl]benzaldehyde
反応式
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[CH2:23]([C:27]1[CH:32]=[CH:31][C:30]([C:33]2[O:37][C:36]([C:38]3[CH:43]=[CH:42][C:41]([CH2:44][OH:45])=[CH:40][CH:39]=3)=[N:35][N:34]=2)=[CH:29][CH:28]=1)[CH:24]([CH3:26])[CH3:25]>ClCCl>[CH2:23]([C:27]1[CH:28]=[CH:29][C:30]([C:33]2[O:37][C:36]([C:38]3[CH:39]=[CH:40][C:41]([CH:44]=[O:45])=[CH:42][CH:43]=3)=[N:35][N:34]=2)=[CH:31][CH:32]=1)[CH:24]([CH3:26])[CH3:25]参加物
4
実験手順
Dess-Martin periodinane (0.576 g, 21.4 mmol) was added to a solution of {4-[5-(4-isobutylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}methanol (0.322 g, 1.04 mmol) and dichloromethane (10 mL) and stirred at room temperature for 1 hour. The reaction mixture was quenched with 1M NaOH (10 mL), stirred for 15 minutes then additional 1N NaOH (5 mL) was added. The layers were separated and the aqueous phase was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (0.322 g, 88% yield) as a white solid.