반응식
[OH:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]([OH:18])=[CH:4][CH:3]=1.B(O)(O)O.[CH3:23][O:24][CH2:25][CH2:26][CH2:27][NH2:28]>O>[CH3:23][O:24][CH2:25][CH2:26][CH2:27][NH:28][C:4]1[CH:3]=[C:2]([OH:1])[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]=1[OH:18].[OH:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]([OH:18])=[CH:4][CH:3]=1참가 물질
6
반응 조건
- 온도
- 65 °C
실험 절차
2-(methoxypropylamino)-1,4-dihydroxyanthraquinone was prepared as follows: 60 grams of 1,4-dihydroxyanthraquinone, 15.5 grams of boric acid, and 89 grams of methoxypropylamine were slurried in 125 ml of water. The slurry was stirred and heated to 65° Celsius, and a strong stream of air was bubbled through it. These conditions were maintained about nine hours, or until thin layer chromatography of the reaction mixture failed to isolate any, 1,4-dihydroxyanthraquinone.
후처리
- customa strong stream of air was bubbled through it
- temperatureThese conditions were maintained about nine hours
출처 및 근거
- ORD 기록
- ord-bdd196d979a84c5da73851f747171d88
- 출처 데이터셋
- uspto-grants-1988_08
- 특허 번호
- US04764474
연결된 노트
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