Chloroform → HCID 29923590, 화합물
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[N+:1]([O-:15])([O:3][CH2:4][C@H:5]([O:11][N+:12]([O-:14])=[O:13])[CH2:6][CH2:7][CH2:8][CH2:9][OH:10])=[O:2].I([O-])(=O)(=O)=[O:17].[Na+].C(#N)C.C(Cl)(Cl)Cl>O.ClCCl.O.[Ru]=O.CO>[N+:12]([O:11][C@@H:5]([CH2:4][O:3][N+:1]([O-:15])=[O:2])[CH2:6][CH2:7][CH2:8][C:9]([OH:17])=[O:10])([O-:14])=[O:13]참가 물질
실험 절차
A mixture of (2R)-6-hydroxyhexane-1,2-diyl dinitrate (13.5 g, 60.2 mmol) and sodium periodate (38.74 g, 181 mmol) was suspended in a mixture of water (250 mL), acetonitrile (250 mL), and chloroform (250 mL). Ruthenium oxide hydrate (0.813 g, 6.11 mmol) was then added, turning the reaction bright yellow. After 16 hours, the reaction mixture was concentrated in vacuo to remove the organic solvents. The residue was extracted with dichloromethane (3×200 mL), and the combined organic extracts were washed with brine, dried (magnesium sulfate), and concentrated in vacuo to afford the crude product. Chromatography over silica eluting with 0-5% methanol in dichloromethane afforded the title compound as a yellow liquid. 1H NMR (500 MHz, CDCl3) 5.26-5.33 (m, 1H), 4.76 (dd, J=3.1, 12.9 Hz, 1H), 4.49 (dd, J=6.4, 13.0 Hz, 1H), 2.45 (t, J=5.8 Hz, 2H), 1.72-1.88 (m, 4H).
후처리
- customthe reaction bright yellow
- concentrationthe reaction mixture was concentrated in vacuo
- customto remove the organic solvents
- extractionThe residue was extracted with dichloromethane (3×200 mL)
- washthe combined organic extracts were washed with brine
- dry with materialdried (magnesium sulfate)
- concentrationconcentrated in vacuo
- customto afford the crude product
출처 및 근거
- ORD 기록
- ord-25661f4c788e4f40bace58b4e01adc89
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07834042B2
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