[3-(methoxymethoxy)-1-(2-methylphenyl)-1H-pyrazol-4-yl]methanol → 3-(methoxymethoxy)-1-(2-methylphenyl)-1H-pyrazole-4-carbaldehyde
反応式
[CH3:1][O:2][CH2:3][O:4][C:5]1[C:9]([CH2:10][OH:11])=[CH:8][N:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:6]=1>[O-2].[O-2].[Mn+4].C1(C)C=CC=CC=1>[CH3:1][O:2][CH2:3][O:4][C:5]1[C:9]([CH:10]=[O:11])=[CH:8][N:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:6]=1参加物
4
実験手順
A mixture of [3-(methoxymethoxy)-1-(2-methylphenyl)-1H-pyrazol-4-yl]methanol (2.39 g), activated manganese dioxide (5.0 g) and toluene (30 mL) was stirred at room temperature for 8 hrs. Activated manganese dioxide (5.0 g) was added and the mixture was further stirred for 12 hrs. Manganese dioxide was removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:9-1:2, v/v) to give 3-(methoxymethoxy)-1-(2-methylphenyl)-1H-pyrazole-4-carbaldehyde as an orange oil (1.65 g, yield 81%).