Diethyl Oxalate → 2,4-Dioxo-4-phenyl-butyric acid ethyl ester
반응식
[Na].[C:2]([O:9][CH2:10][CH3:11])(=[O:8])[C:3]([O:5]CC)=O.[C:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:14])[CH3:13]>C(O)C>[C:12]([CH2:13][C:3](=[O:5])[C:2]([O:9][CH2:10][CH3:11])=[O:8])(=[O:14])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1참가 물질
실험 절차
In 560 ml of ethanol was dissolved 25 g (1.08 eq.) of sodium and a mixture of 135.6ml (146 g; 1 mol) of diethyl oxalate and 116.7 ml (120 g; 1 mol) of acetophenone was added thereto dropwise at 40° C. One hour later, reflux was begun and it was continued for 30 minutes. The solvent was distilled off. The residue was neutralized with sulfuric acid (55 g/water 200 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. Thereafter, the solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent: dichloromethane/hexane 1:1), to give colorless plates. The crystals were recovered by filtration with ethyl acetate/hexane. Yield: 114.6 g.
후처리
- additionwas added
- customdropwise at 40° C
- temperatureOne hour later, reflux
- distillationThe solvent was distilled off
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with water
- dry with materiala saturated aqueous solution of sodium chloride, and dried over magnesium sulfate
- distillationThereafter, the solvent was distilled off
- customthe residue was purified by silica gel column chromatography (eluent: dichloromethane/hexane 1:1)
- customto give colorless plates
- filtrationThe crystals were recovered by filtration with ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-f711d3437ac74f85b47876be8d6e5fe7
- 출처 데이터셋
- uspto-grants-1995_05
- 특허 번호
- US05420275
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