반응식
[Mg].[C:2]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH2:13]([CH:16]1[CH2:21][CH2:20][CH:19]([C:22](Cl)=[O:23])[CH2:18][CH2:17]1)[CH2:14][CH3:15].OS(O)(=O)=O>CCO.C1(C)C=CC=CC=1.[Cl-].[Na+].O.C(Cl)(Cl)(Cl)Cl>[CH2:11]([O:10][C:2](=[O:9])[CH:3]([C:22]([CH:19]1[CH2:20][CH2:21][CH:16]([CH2:13][CH2:14][CH3:15])[CH2:17][CH2:18]1)=[O:23])[C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:12]참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
실험 절차
To 2.5 mL of anhydrous EtOH and 0.25 mL carbon tetrachloride was added 1.2 g (50 mmol) magnesium turnings. 8.0 g (50 mmol) diethyl malonate was dissolved in a mixture of 5 mL anhydrous EtOH and 20 mL anhydrous toluene and added in small portions to the magnesium turnings over the course of 1.5 hr so as to maintain a gentle reflux. The reaction was stirred at room temperature for 1 hr, and then cooled to 0° C. in ice. 4-Propyl-cyclohexanecarbonyl chloride (50 mmol) was added dropwise and the reaction was allowed to warm to room temperature over night. The reaction was then heated to 55° C. for 4 hr with stirring, allowed to cool to ambient temperature, and was poured into a slurry of crushed ice and 10% H2SO4. The solution was diluted with brine and extracted with ethyl acetate. The organic layer was separated, dried over MgSO4, and concentrated to afford 10.71 g (34.28 mmol) 2-(4-propyl-cyclohexanecarbonyl)-malonic acid diethyl ester as a clear, near colorless oil.
후처리
- temperatureto maintain a gentle reflux
- temperaturecooled to 0° C. in ice
- temperatureto warm to room temperature over night
- temperatureThe reaction was then heated to 55° C. for 4 hr
- stirringwith stirring
- temperatureto cool to ambient temperature
- extractionextracted with ethyl acetate
- customThe organic layer was separated
- dry with materialdried over MgSO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-44c439965f4b4537b0c76da3e33c7e09
- 출처 데이터셋
- uspto-grants-2009_02
- 특허 번호
- US07488832B2
연결된 노트
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