7-(1,1-Dimethylethyl)-2,3-benzofurandione → HCID 23043620, 화합물
반응식
[CH3:1][C:2]([C:5]1[C:13]2[O:12][C:11](=[O:14])[C:10](=[O:15])[C:9]=2[CH:8]=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH2:26][CH2:27][C:28]2[CH:33]=[CH:32][C:31]([NH2:34])=[CH:30][CH:29]=2)[CH:21]=[CH:22][C:23]=1[O:24][CH3:25]>ClCCl>[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH2:26][CH2:27][C:28]2[CH:29]=[CH:30][C:31]([NH:34][C:11](=[O:14])[C:10](=[O:15])[C:9]3[CH:8]=[CH:7][CH:6]=[C:5]([C:2]([CH3:4])([CH3:3])[CH3:1])[C:13]=3[OH:12])=[CH:32][CH:33]=2)[CH:21]=[CH:22][C:23]=1[O:24][CH3:25]참가 물질
4
실험 절차
A solution of 7-(1,1-dimethylethyl)-2,3-benzofurandione (1.0 g, 5 mmol) and 4-[2-(3,4-dimethoxyphenyl)ethyl]benzenamine (1.0 g, 4 mmol) in 10 ml of dichloromethane is stirred at room temperature for 48 hours. The solvent is evaporated and the residue crystallized from ether/hexane. Recrystallization from acetonitrile gave the pure product, (1.0 g) mp 143°-144° C.
후처리
- customThe solvent is evaporated
- customthe residue crystallized from ether/hexane
- customRecrystallization from acetonitrile
- customgave the pure product, (1.0 g) mp 143°-144° C.
출처 및 근거
- ORD 기록
- ord-6829ea3438db41e099418e4702b7b03b
- 출처 데이터셋
- uspto-grants-1990_07
- 특허 번호
- US04939133
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