Methyl 6-dimethylamino-4,4-diphenyl-2-heptenoate → Methyl 6-dimethylamino-4,4-diphenyl-heptanoate
反応式
[CH3:1][N:2]([CH3:25])[CH:3]([CH3:24])[CH2:4][C:5]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:6]=[CH:7][C:8]([O:10][CH3:11])=[O:9]>[Pd].CO>[CH3:25][N:2]([CH3:1])[CH:3]([CH3:24])[CH2:4][C:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)[CH2:6][CH2:7][C:8]([O:10][CH3:11])=[O:9]参加物
4
実験手順
A mixture of methyl 6-dimethylamino-4,4-diphenyl-2-heptenoate (60 mg), 10% Pd/C (10 mg), and methanol was hydrogenated at room temperature for 18 hours. The mixture was filtered through a short pad of celite, and the filtrate was rotary evaporated to give methyl 6-dimethylamino-4,4-diphenyl-heptanoate, as a crude material which was then dried in vacuo.
後処理
- filtrationThe mixture was filtered through a short pad of celite
- customthe filtrate was rotary evaporated
出典と根拠
- ORDレコード
- ord-d0420531e88d43e4ae9d467af14c0539
- 出典データセット
- uspto-grants-1991_12
- 特許番号
- US05073629
反応ノート
読み込み中…