Sodium periodate → 1-Tert-butyl 4-methyl 4-(2-oxopropyl)piperidine-1,4-dicarboxylate
반응식
[CH3:1][C:2](=C)[CH2:3][C:4]1([C:17]([O:19][CH3:20])=[O:18])[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1.I([O-])(=O)(=O)=[O:23].[Na+]>O1CCOCC1.O.ClCCl.[Os](=O)(=O)(=O)=O>[O:23]=[C:2]([CH3:1])[CH2:3][C:4]1([C:17]([O:19][CH3:20])=[O:18])[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1참가 물질
6
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
To a solution of 1-tert-butyl 4-methyl 4-(2-methylallyl)piperidine-1,4-dicarboxylate (2.2 g, 7.4 mmol) in dioxane/water (60 mL, 1/1) under nitrogen was added osmium tetroxide (0.038 g, 0.15 mmol) and sodium periodate (2.88 g, 13.5 mmol). The mixture was stirred at room temperature for 3 hours. The mixture was then diluted with dichloromethane (50 mL), and washed with 20% Na2S2O3 (20 mL). The organic layers were combined and washed with brine (20 mL), dried over anhydrous sodium sulfate, and filtered. The filtrates were concentrated and the residue was purified by column chromatography eluting with 0-60% ethyl acetate/hexane to afford 1-tert-butyl 4-methyl 4-(2-oxopropyl)piperidine-1,4-dicarboxylate. LC-MS (IE, m/z): 322.26 (M+23)+.
후처리
- washwashed with 20% Na2S2O3 (20 mL)
- washwashed with brine (20 mL)
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationThe filtrates were concentrated
- customthe residue was purified by column chromatography
- washeluting with 0-60% ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-26c5fd124d5c4401aa671d22ac9ab6e6
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08952166B2
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