Water → 2-Methoxy-4-methylpyridine
Reaktionsgleichung
Cl[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.[O:9]([CH3:11])[Na].O>CS(C)=O>[CH3:11][O:9][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
A mixture of 2-chloro-4-methylpyridine (20 g, 0.156 mol) and NaOCH3 (9.3 g, 0.172 mol) in DMSO (200 mL) was stirred at 100° C. for 4 hours. The solution was added to H2O and then extracted with ethyl acetate (50 mL×2). The organic layer was washed with H2O (300 mL) brine (300 mL) and dried concentrated to give 2-methoxy-4-methylpyridine (9 g, 46%). LC-MS: 124 [M+H]+, tR=1.21 min.
Aufarbeitung
- extractionextracted with ethyl acetate (50 mL×2)
- washThe organic layer was washed with H2O (300 mL) brine (300 mL)
- customdried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-a0838bff0a754ad09f228882450d6756
- Quelldatensatz
- uspto-grants-2014_12
- Patentnummer
- US08921383B2
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