trans-3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]-5-methylcyclohexanone → trans-3-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]-5-methyl-cyclohexanone
反応式
C([O:8][C:9]1[CH:14]=[C:13]([C:15]([CH3:23])([CH3:22])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH:12]=[CH:11][C:10]=1[C@H:24]1[CH2:29][C@H:28]([CH3:30])[CH2:27][C:26](=[O:31])[CH2:25]1)C1C=CC=CC=1.[H][H]>[Pd].CO>[CH3:23][C:15]([C:13]1[CH:12]=[CH:11][C:10]([C@H:24]2[CH2:29][C@H:28]([CH3:30])[CH2:27][C:26](=[O:31])[CH2:25]2)=[C:9]([OH:8])[CH:14]=1)([CH3:22])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]参加物
5
実験手順
A mixture of trans-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-5-methylcyclohexanone (175 mg, 0.417 mmole) and 175 mg of 5% palladium on carbon-50% water in methanol (8 ml) was stirred under one atmosphere of hydrogen gas until hydrogen uptake ceased. The reaction mixture was filtered through diatomaceous earth and the filtrate evaporated under reduced pressure. Crystallization of the residue in pentane gave 89 mg (64%) of the title compound.
後処理
- filtrationThe reaction mixture was filtered through diatomaceous earth
- customthe filtrate evaporated under reduced pressure
- customCrystallization of the residue in pentane
出典と根拠
- ORDレコード
- ord-b71aa945531446ee8485959bfd829f13
- 出典データセット
- uspto-grants-1981_12
- 特許番号
- US04306097
反応ノート
読み込み中…