반응식
[CH:1]([C:4]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([CH3:13])[CH3:12])[C:5]=1[NH2:6])([CH3:3])[CH3:2].C1([O-])C=CC=CC=1.[CH:21]1[C:34]2[C:25](=[CH:26][C:27]3[C:32]([C:33]=2[C:35]2[CH:40]=[C:39]([CH3:41])[CH:38]=[CH:37][C:36]=2[OH:42])=[CH:31][CH:30]=[CH:29][CH:28]=3)[CH:24]=[CH:23][CH:22]=1.[OH-].[Na+].[N:45]1C=CC=CC=1>C1C=CC=CC=1.O>[CH:11]([C:7]1[CH:8]=[CH:9][CH:10]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5]=1[N:6]=[N:45][C:37]1[CH:38]=[C:39]([CH3:41])[CH:40]=[C:35]([C:33]2[C:34]3[C:25]([CH:26]=[C:27]4[C:32]=2[CH:31]=[CH:30][CH:29]=[CH:28]4)=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:36]=1[OH:42])([CH3:13])[CH3:12]참가 물질
8
실험 절차
This phenol was prepared, as described above, from a theoretical yield of 3.9 mmol of diazotized 2,6-diisopropylaniline and a phenolate solution comprised of 2-(9-Anthracenyl)-4-methylphenol (0.63 g), water (20 mL), NaOH (20 mmol), pyridine (2 mL), and benzene (4 mL). In this case, the product was eluted with ether:hexanes (1:10). Yield=0.30 g (29%).
후처리
- washIn this case, the product was eluted with ether:hexanes (1:10)
출처 및 근거
- ORD 기록
- ord-966493f923fe4472bb4fc0c0429b9e71
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07094848B2
연결된 노트
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