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[OH:1]N1[C:6](=[O:7])[C:5]2=CC=CC=C2C1=O.[C:13]([C:16]12[CH2:26][C:20]3([CH3:27])[CH2:21][C:22]([OH:25])([CH2:24][C:18]([CH3:28])([CH2:19]3)[CH2:17]1)[CH2:23]2)(=[O:15])[CH3:14]>>[C:13]([C:16]12[CH2:26][C:20]3([CH3:27])[CH2:21][CH:22]([CH2:24][C:18]([CH3:28])([CH2:19]3)[CH2:17]1)[CH2:23]2)(=[O:15])[CH3:14].[C:13]([C:16]12[CH2:26][C:20]3([CH3:27])[CH2:19][C:18]([CH3:28])([CH2:24][C:22]([C:6](=[O:7])[CH3:5])([CH2:21]3)[CH2:23]1)[CH2:17]2)(=[O:15])[CH3:14].[CH3:13][C:16]12[CH2:23][C:22]3([OH:25])[CH2:24][CH:18]([CH2:19][C:20]([CH3:27])([CH2:21]3)[CH2:26]1)[CH2:17]2.[CH3:27][C:20]12[CH2:21][CH:22]3[CH2:23][CH:16]([CH2:17][C:18]([CH3:28])([C:24]3=[O:1])[CH2:19]1)[CH2:26]2참가 물질
6
실험 절차
Except that the amount of N-hydroxyphthalimide was changed to 0.6 mmol, the procedure of Example 9 was repeated to give 1-acetyl-3,5-dimethyladamantane (yield 32%, selectivity 54%), 1,3-diacetyl-5,7-dimethyladamantane (yield 2%, selectivity 3%), 1-acetyl-3,5-dimethyl-7-adamantanol (yield %, selectivity 2%), 1,3-dimethyl-5-adamantanol (yield 7%, selectivity 12%), and 1,3-dimethyl-4-adamantanone (yield 5%, selectivity 8%), at a conversion rate from 1,3-dimethyladamantane of 59%.
출처 및 근거
- ORD 기록
- ord-7d1ff4c668d94946a51b76cdc3322555
- 출처 데이터셋
- uspto-grants-2002_08
- 특허 번호
- US06429314B1
연결된 노트
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