N-Methylmorpholine N-oxide monohydrate → HCID 21948859, Verbindung

HRID 2182695Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2182695
[OH2:1].[CH3:2][N+:3]1([O-])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[N+:10]([C:13]1[CH:22]=[CH:21]C=C2[C:14]=1[CH:15]=[CH:16]C(C=C)=N2)([O-:12])=[O:11]>C(O)(C)C.CC(C)=O.O.[Os](=O)(=O)(=O)=O>[OH:1][CH:8]([N:3]1[C:4]2[C:14](=[C:13]([N+:10]([O-:12])=[O:11])[CH:22]=[CH:21][CH:5]=2)[CH:15]=[CH:16][CH2:2]1)[CH2:7][OH:6]

Komponenten

7

Versuchsvorschrift

336 mg (2.5 mmol) of N-methylmorpholine-N-oxide hydrate and 10.22 ml of osmium tetroxide solution in isopropanol are added at 0° C. to a solution that consists of 3.18 g (15.88 mmol) of 5-nitro-2-vinylquinoline in 140 ml of acetone and 21 ml of water, and the reaction mixture is stirred for 24 hours at room temperature. Then, the solvent is removed in a vacuum, and the residue is taken up in ethyl acetate. The organic phase is washed with water and saturated sodium chloride solution. The aqueous phase is extracted repeatedly with dichloromethane, diethyl ether and ethyl acetate. The combined organic phases are dried on sodium sulfate. After removal of the solvent and purification of silica gel with hexane-ethyl acetate (0-100%) as well as with ethyl acetate-methanol (0-20%), 1.64 g (44% of theory) of the product is obtained.

Aufarbeitung

  1. customThen, the solvent is removed in a vacuum
  2. washThe organic phase is washed with water and saturated sodium chloride solution
  3. extractionThe aqueous phase is extracted repeatedly with dichloromethane, diethyl ether and ethyl acetate
  4. customThe combined organic phases are dried on sodium sulfate
  5. customAfter removal of the solvent and purification of silica gel with hexane-ethyl acetate (0-100%) as well as with ethyl acetate-methanol (0-20%), 1.64 g (44% of theory) of the product
  6. customis obtained

Quellen und Nachweise

ORD-Eintrag
ord-ce0a04d964694cad9094c952ca23feea
Quelldatensatz
uspto-grants-2005_05
Patentnummer
US06897224B2

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