Diethyl Malonate → HCID 15097258, 화합물
반응식
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[O-]CC.[Na+].[Na].Br[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][O:23][CH2:24][O:25][CH2:26][CH2:27][O:28][CH3:29]>C(O)C>[CH3:29][O:28][CH2:27][CH2:26][O:25][CH2:24][O:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:1]([O:9][CH2:10][CH3:11])=[O:8]참가 물질
실험 절차
A solution of 37.80 of diethyl malonate dissolved in 20 ml of absolute ethanol was added dropwise to a solution of sodium ethoxide prepared by gradually adding 3.00 g of metallic sodium to 30 ml of absolute ethanol. To the mixture was added a solution of 30.01 g of 1-bromo-5-(2-methoxyethoxy)methoxypentane (prepared as described in Preparation 60) dissolved in 10 ml of absolute ethanol. The mixture was heated under reflux for 21 hours, after which it was allowed to cool, and then the solvent was distilled off. The residue was mixed with water, and the mixture was extracted three times with ethyl acetate. The combined extracts were washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 850 g of silica gel, and 32.78 g of the title compound were obtained, as a colorless oil, from those fractions eluted with a 4:1 by volume mixture of hexane and ethyl acetate.
후처리
- customprepared
- temperatureThe mixture was heated
- temperatureunder reflux for 21 hours
- temperatureto cool
- distillationthe solvent was distilled off
- additionThe residue was mixed with water
- extractionthe mixture was extracted three times with ethyl acetate
- washThe combined extracts were washed with water
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated by evaporation under reduced pressure
출처 및 근거
- ORD 기록
- ord-9c188e9f828645758836b8d617beb312
- 출처 데이터셋
- uspto-grants-1990_01
- 특허 번호
- US04891363
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