Reaktionsgleichung
[Br:1][C:2]1[C:3](F)=[N:4][CH:5]=[CH:6][CH:7]=1.[CH3:9][C:10]([CH3:13])([O-:12])[CH3:11].[K+]>O1CCCC1>[Br:1][C:2]1[C:3]([O:12][C:10]([CH3:13])([CH3:11])[CH3:9])=[N:4][CH:5]=[CH:6][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-bromo-2-fluoropyridine (500 mg, 2.84 mmol) in anhydrous tetrahydrofuran (10 mL) under nitrogen was added potassium tert-butoxide (540 mg, 4.8 mmol) in portions over 30 minutes at 25° C., and stirring was continued for 4 hours at 25° C. The mixture was concentrated in vacuo and purified by silica gel flash chromatography eluting with dichloromethane/hexanes (50% to 100%) to give the title compound.
Aufarbeitung
- concentrationThe mixture was concentrated in vacuo
- custompurified by silica gel flash chromatography
- washeluting with dichloromethane/hexanes (50% to 100%)
Quellen und Nachweise
- ORD-Eintrag
- ord-0763c82d1c184bd2a568fb0059e68e7a
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08748443B2
Verknüpfte Notizen
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