Reaktionsgleichung
[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][N:4]=1.C([O-])(O)=O.[Na+].[Br:16]Br>ClCCl>[Br:16][C:6]1[CH:7]=[C:8]([O:9][CH3:10])[C:3]([O:2][CH3:1])=[N:4][CH:5]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
To a solution of 2,3-dimethoxypyridine (4-1, 2.5 g, 18.0 mmol, 1.0 equiv) in dichloromethane:saturated NaHCO3 (80 mL: 40 mL) at 0° C. was added bromine (0.93 mL, 18.0 mmol, 1.0 equiv) and the reaction mixture was stirred for 2 h at 25° C. The reaction mixture was quenched with solid Na2SO3 (˜10 g) and the aqueous phase was extracted with dichloromethane (3×100 mL). The organic phase was dried over magnesium sulfate and concentrated. The residue was purified via normal phase chromatography (0 to 20% EtOAc in hexanes, silica) to afford the desired product (4-2) as an oil after concentration. ESI+MS[M+H]+C7H8NO2 calc'd 218.0. found 218.0.
Aufarbeitung
- customThe reaction mixture was quenched with solid Na2SO3 (˜10 g)
- extractionthe aqueous phase was extracted with dichloromethane (3×100 mL)
- dry with materialThe organic phase was dried over magnesium sulfate
- concentrationconcentrated
- customThe residue was purified via normal phase chromatography (0 to 20% EtOAc in hexanes, silica)
Quellen und Nachweise
- ORD-Eintrag
- ord-431d313e6da14df89a9f365c33d5ca1f
- Quelldatensatz
- uspto-grants-2013_11
- Patentnummer
- US08592457B2
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