반응식
[CH2:1]([CH:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:2].[H-].[Na+].[CH2:16]([O:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][CH2:31]I)=[CH:26][CH:25]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.O>CN(C)C=O.O1CCCC1>[CH2:1]([C:3]([CH2:31][CH2:30][C:27]1[CH:28]=[CH:29][C:24]([O:23][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:25][CH:26]=1)([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]참가 물질
실험 절차
Diethyl ethylmalonate (50 g) was added to a suspension of sodium hydride (11 g) in dimethylformamide (200 ml) and tetrahydrofuran (50 ml), at 0° C., and the mixture was stirred at room temperature for 35 minutes. A solution of 2-(4-benzyloxyphenyl)ethyl iodide (90 g) was added to the reaction mixture at 0° C. and the whole mixture was stirred at 0° C. for 20 minutes and allowed to stand at room temperature overnight. The resultant mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and a saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:9) to give the subject compound (100 g).
후처리
- stirringthe whole mixture was stirred at 0° C. for 20 minutes
- waitto stand at room temperature overnight
- extractionextracted with ethyl acetate
- washThe ethyl acetate layer was washed with water
- dry with materiala saturated brine and dried over anhydrous magnesium sulfate
- distillationThe solvent was distilled away under reduced pressure
- customthe residue obtained
- customwas purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:9)
출처 및 근거
- ORD 기록
- ord-2e0d65b3992d40be9ce140d1f4adc5e9
- 출처 데이터셋
- uspto-grants-2001_02
- 특허 번호
- US06187821B1
연결된 노트
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