Methyl morpholine oxide → 2-[(1R,2S,3R)-2,3-dihydroxycyclohexyl]-1H-isoindole-1,3(2H)-dione
Reaktionsgleichung
[C@@H:1]1([N:7]2[C:15](=[O:16])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8]2=[O:17])[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.C[N+]1([O-])CC[O:22]CC1.CC(C)=O.[OH2:30]>[Os](=O)(=O)(=O)=O>[OH:30][C@@H:2]1[C@H:3]([OH:22])[CH2:4][CH2:5][CH2:6][C@H:1]1[N:7]1[C:15](=[O:16])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]1=[O:17]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 2-[(1R)-cyclohex-2-en-1-yl]-1H-isoindole-1,3(2H)-dione (18) (19.9 mmol, 4.53 g) and 4-methylmorpholine-N-oxide (60 mmol, 7.01 g) in acetone/water (4:1, 62.5 mL), osmium tetroxide (0.2 mmol, 50 mg) was added. The reaction was stirred for 4 h. The mixture was concentrated and saturated sodium sulfite (40 mL) was added. It was then promptly extracted with EtOAc three times. The combined organic layers were washed with water and brine, dried over MgSO4 and concentrated to give the crude product as a white solid (4.94 g, 95% yield). Chiral HPLC [8.53 min]. Analytical data matched published data (Donohoe, J. T.; et al., J. Org. Chem., 2002, 67, 7946-7956)
Aufarbeitung
- additionwas added
- concentrationThe mixture was concentrated
- additionsaturated sodium sulfite (40 mL) was added
- extractionIt was then promptly extracted with EtOAc three times
- washThe combined organic layers were washed with water and brine
- dry with materialdried over MgSO4
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-0d962995f39542ec8daa9ecf265cd1ae
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08889719B2
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