Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[O-].CC[O:11][C:12]([CH3:14])=[O:13]>C(OC(=O)C)(=O)C>[C:12]([O:13][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1)(=[O:11])[CH3:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of the 2-methylpyridine N-oxide (1.0 mmol) in acetic anhydride (5 mL) was heated to reflux for 0.5 h. Work-up (EtOAc), drying (MgSO4), evaporation and purification by preparative TLC or flash chromatography afforded the 2-(acetoxymethyl) pyridine.
Aufarbeitung
- temperatureto reflux for 0.5 h
- customdrying
- custom(MgSO4), evaporation and purification by preparative TLC or flash chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-f83b1c34a6e84d08b42a25dcbe21d002
- Quelldatensatz
- uspto-grants-2006_11
- Patentnummer
- US07138402B2
Verknüpfte Notizen
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