Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([C@H:8](O)[CH3:9])[CH:5]=[N:6][CH:7]=1.C1(P([N:25]=[N+:26]=[N-:27])(C2C=CC=CC=2)=O)C=CC=CC=1.N12CCCN=C1CCCCC2>O1CCCC1.C(OCC)(=O)C.O>[N:25]([C@H:8]([C:4]1[CH:5]=[N:6][CH:7]=[C:2]([Br:1])[CH:3]=1)[CH3:9])=[N+:26]=[N-:27]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
To a solution of (1R)-1-(5-bromopyridin-3-yl)ethanol (10 mmol) in tetrahydrofuran (40 mL), cooled to 0° C., was added diphenylphosphoryl azide (4.3 mL, 20 mmol) in one portion followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (3 mL, 20 mmol) dropwise over 30 minutes. After this time the reaction mixture was allowed to warm slowly to room temperature and was stirred overnight. The mixture was diluted with ethyl acetate (50 mL) and water (50 mL), the two phases separated and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phases were washed with brine (50 mL), dried (MgSO4) and concentrated under reduced pressure to give a black liquid which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 3-[(1S)-1-azidoethyl]-5-bromopyridine (1.7 g, 75%) as a colourless liquid.
Aufarbeitung
- customthe two phases separated
- extractionthe aqueous phase extracted with ethyl acetate (3×50 mL)
- washThe combined organic phases were washed with brine (50 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated under reduced pressure
- customto give a black liquid which
- customwas purified by flash chromatography (silica, ethyl acetate/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-4db8b242fd664bfd922465040967c31a
- Quelldatensatz
- uspto-grants-2013_06
- Patentnummer
- US08461161B2
Verknüpfte Notizen
Wird geladen…