Dimethylformamide → HCID 18594803, 화합물
반응식
CS(O[CH:6]([CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:7][CH2:8][C@@H:9]1[C@@H:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:12](=[O:25])[CH2:11][CH2:10]1)(=O)=O.CN(C)C=O.[Cl-:36].[Li+]>O>[Cl:36][CH:6]([CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:7][CH2:8][C@@H:9]1[C@@H:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:12](=[O:25])[CH2:11][CH2:10]1참가 물질
5
실험 절차
A solution of 1.35 g. of ethyl 15-methanesulfonyloxy 9-oxo-prostanoate (Example 90) in 40 ml. of N,N-dimethylformamide containing 650 mg. of lithium chloride is heated on the steam bath for 18 hours. The cooled solution is diluted with water and the resulting mixture is extracted with ether. The ether extract is washed with saline, dried with saline, dried with anhydrous magnesium sulfate and evaporated to dryness to give an oil. Chromatography on silica gel affords an oil; λmax. 5.78 μ (carbonyl groups).
후처리
- extractionthe resulting mixture is extracted with ether
- extractionThe ether extract
- washis washed with saline
- customdried with saline
- dry with materialdried with anhydrous magnesium sulfate
- customevaporated to dryness
- customto give an oil
- customChromatography on silica gel affords an oil
출처 및 근거
- ORD 기록
- ord-11bb2503511e402c905725720c09bf80
- 출처 데이터셋
- uspto-grants-1976_01
- 특허 번호
- US03932472
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