반응식
[H-].[Na+].CC(C)([O-])C.[K+].[C:9](=[O:14])([O:12][CH3:13])OC.[C:15]1(=[O:26])[C:20]2([CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[CH2:19][CH2:18][CH2:17][CH2:16]1>O1CCCC1.[Cl-].[Na+].O.C(O)(=O)C>[CH3:13][O:12][C:9]([CH:16]1[CH2:17][CH2:18][CH2:19][C:20]2([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]2)[C:15]1=[O:26])=[O:14]참가 물질
실험 절차
To a suspension of 60% sodium hydride (5.7 g) and potassium tert-butoxide (1.6 g) in tetrahydrofuran (200 mL) was added dimethyl carbonate (9.6 mL) at room temperature while stirring. The reaction mixture was heated under reflux. To the reaction mixture was added dropwise a solution of spiro[5.5]undecan-1-one (11.85 g) obtained in Step 1 in tetrahydrofuran (40 mL) over 1 hour, followed by heating the reaction mixture under reflux for 2 hours. After ice-cooling, acetic acid (14.6 mL) was added dropwise to the reaction mixture. Then, the reaction mixture was poured into saturated brine, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:15) to give 1-oxo-spiro[5.5]undecane-2-carboxylic acid methyl ester (13.02 g).
후처리
- temperatureThe reaction mixture was heated
- temperatureunder reflux
- temperatureby heating the reaction mixture
- temperatureunder reflux for 2 hours
- temperatureAfter ice-cooling
- extractionfollowed by extraction with ethyl acetate
- washThe organic layer was washed with saturated brine
- customdried
- concentrationconcentrated
- customThe residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:15)
출처 및 근거
- ORD 기록
- ord-65f5429401d14c5d9d02ae3beff46eda
- 출처 데이터셋
- uspto-grants-2012_10
- 특허 번호
- US08299296B2
연결된 노트
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