반응식
[CH3:1][N:2]([CH2:4][CH2:5][CH:6]([OH:12])[C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH3:3].[OH-].[K+].F[C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:19]=[CH:18][CH:17]=1.[C:26]([OH:35])(=[O:34])[C@H:27]([C@@H:29]([C:31]([OH:33])=[O:32])[OH:30])[OH:28]>CS(C)=O.O>[CH3:1][N:2]([CH2:4][CH2:5][CH:6]([O:12][C:24]1[C:25]2[C:20](=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:21]=[CH:22][CH:23]=1)[C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH3:3].[C:31]([C@H:29]([C@@H:27]([C:26]([O-:35])=[O:34])[OH:28])[OH:30])([O-:33])=[O:32]참가 물질
7
반응 조건
- 온도
- 110 °C
실험 절차
A mixture of N,N-dimethyl-3-hydroxy-3-(2-thienyl)propylamine (185 g, 1 mole), potassium hydroxide (112 g, 2 moles) and 1-fluoronaphthalene (146 g, 1 mole) in dimethylsulfoxide (1000 ml) is stirred at 110° C. for 2 hours. After cooling down to 20° C., the mixture is filtered, diluted with water (3 l), D-tartaric acid (75 g, 0.5 mole) is added and the mixture is stirred at 80° C. for 0.5 hour. After cooling down, the precipitated product is sucked off, washed with water and dried. Yield: 313 g (81%).
후처리
- temperatureAfter cooling down to 20° C.
- filtrationthe mixture is filtered
- additionis added
- stirringthe mixture is stirred at 80° C. for 0.5 hour
- temperatureAfter cooling down
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-1f1d09bc99434a4088561b4461739bef
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08207356B2
연결된 노트
불러오는 중…