반응식
CN(C)[CH:3]=[O:4].[OH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]1[C:32]([OH:33])=[C:31]([O:34][CH3:35])[C:30]([O:36][CH3:37])=[CH:29][C:28]=1C>O=O.C1C=C(C=NCCN=CC2C([O-])=CC=CC=2)C([O-])=CC=1.[Co+2]>[OH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]1[C:32](=[O:33])[C:31]([O:34][CH3:35])=[C:30]([O:36][CH3:37])[C:3](=[O:4])[C:28]=1[CH3:29]참가 물질
5
실험 절차
To a dimethylformamide solution (50 ml) of 6-(20-hydroxyeicosanyl)-2,3-dimethoxy-5-methylphenol (4.0 g) is added bis(salicylidene)ethylenediiminocobalt(II) (40 mg), and the mixture is stirred in oxygen streams at atmospheric temperature and pressure for 72 hours. The product is isolated as in Example 7 and recrystallized from ether. The above procedure yields 6-(20-hydroxyeicosyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (3.28 g) as yellow needles melting at 85° C.
후처리
- customThe product is isolated as in Example 7
- customrecrystallized from ether
출처 및 근거
- ORD 기록
- ord-2c2f900c296845b9b095355b03bb20c7
- 출처 데이터셋
- uspto-grants-1985_12
- 특허 번호
- US04559177
연결된 노트
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