1,1'-(1,1-Dimethyl-3-methylene-1,3-propanediyl)bisbenzene → Benzene, 1,1'-(1,1,3-trimethyl-1,3-propanediyl)bis-
反応式
[H][H].[C:3]1([C:9]([CH2:11][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)([CH3:14])[CH3:13])=[CH2:10])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C1COCC1>[C:15]1([C:12]([CH3:14])([CH2:11][CH:9]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH3:10])[CH3:13])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
4
実験手順
In Example 3, hydrogenation reaction was conducted under the same condition as Example 1 for THF diluted solution concentration of the substance to be reduced, its flow rate, and hydrogen 9 flow rate, using 2,4-diphenyl-4-methyl-1-pentene as the substance to be reduced. The reaction time was within five minutes. The analytical result of the reaction product by 1H-NMR showed almost complete hydrogenation of 2,4-diphenyl-4-methyl-1-pentene, and 2,4-diphenyl-2-methylpentane was obtained at about 100% yield (See FIG. 6.).