Oxalic Acid → Adamantanone
반응식
[C:1]([OH:6])(=O)[C:2](O)=[O:3].S(=O)(=O)(O)O.[CH:12]12[CH2:21][CH:16]3C[CH:18]([CH2:20][CH:14]([CH2:15]3)[CH2:13]1)[CH2:19]2>>[CH:16]12[CH2:21][CH:12]3[CH2:13][CH:14]([CH2:20][CH:2]([CH2:19]3)[C:1]1=[O:6])[CH2:15]2.[OH:6][C:1]12[CH2:21][CH:12]3[CH2:13][CH:14]([CH2:20][CH:18]([CH2:19]3)[C:2]1=[O:3])[CH2:15]2참가 물질
5
실험 절차
The reaction was conducted in the same manner as Example 1 except using 1 mmol of oxalic acid instead of 98% by weight of sulfuric acid, the pH of the mixture was 3.7, and as a result, adamantane was converted into adamantanone (yield 8%) and 1-hydroxyadamantanone (yield 2%) with a conversion of 99%. Incidentally, excepting the above, 1-adamantanol (yield 26%), 1,3-adamantanediol (yield 33%) and other products (polyol such as adamantanetriol) (yield 30%) were formed.
출처 및 근거
- ORD 기록
- ord-29bbad28e2c64e2c9d288b3b3b9ae291
- 출처 데이터셋
- uspto-grants-2001_05
- 특허 번호
- US06232258B1
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