반응식
C(N(S(F)(F)[F:7])CC)C.[F:10][CH2:11][C@@H:12]1[C@@H:16]([C:17]2[CH:22]=[CH:21][C:20]([S:23]([CH3:25])=O)=[CH:19][CH:18]=2)[O:15][C:14]([CH3:27])([CH3:26])[N:13]1[C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29].C(=O)(O)[O-].[Na+]>ClCCl.[Sb](Cl)(Cl)Cl>[F:10][CH2:11][C@@H:12]1[C@@H:16]([C:17]2[CH:22]=[CH:21][C:20]([S:23][CH2:25][F:7])=[CH:19][CH:18]=2)[O:15][C:14]([CH3:27])([CH3:26])[N:13]1[C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A solution of diethylamino sulfurtrifluoride (DAST), (9.34 g, 1.75 eq ) in 10 ml of dichloromethane was added drop wise to the solution of 14 (12.3 g) and antimony (III) chloride (0.23 g, 0.03 eq ) in 150 ml of dichloromethane (anhydrous) at −5° C., and the reaction mixture was warmed up to room temperature overnight. A cold saturated solution of sodium bicarbonate (80 ml) was added and stirred for 30 min and extracted with dichloromethane (100 ml×2). The organic layer was washed with a 10% solution of sodium bicarbonate and with brine (50 ml) and dried over sodium sulfate. After purification, via a column, 10.7 g of the desired product (as a heavy oil) was obtained.
후처리
- extractionextracted with dichloromethane (100 ml×2)
- washThe organic layer was washed with a 10% solution of sodium bicarbonate and with brine (50 ml)
- dry with materialdried over sodium sulfate
- customAfter purification
출처 및 근거
- ORD 기록
- ord-ebb033e654d74be2a94b18917bab6ff1
- 출처 데이터셋
- uspto-grants-2008_04
- 특허 번호
- US07361689B2
연결된 노트
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