Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N+:3]=1[O-].[C:10]([O:13]C(=O)C)(=[O:12])[CH3:11]>>[C:10]([O:13][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1)(=[O:12])[CH3:11]Komponenten
3
Versuchsvorschrift
A solution of 2,6-dimethylpyridine 1-oxide (980 mg, 0.79 mmol) in acetic anhydride (5 mL) was refluxed for 1 h. The reaction mixture was then concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography using 20% ethyl acetate in hexanes to afford (6-methylpyridin-2-yl)methyl acetate (1.0 g) as a solid.
Aufarbeitung
- concentrationThe reaction mixture was then concentrated in vacuo
- customto obtain the crude product
- customThe crude material was purified via silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-52430759164042b49e3b56f82a9aa8ff
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08481534B2
Verknüpfte Notizen
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