Reaktionsgleichung
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][N+:7]([O-])=[CH:6][CH:5]=1)[CH3:2].CC(OC(C)=O)=[O:13]>>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][N:7]=[C:6]([OH:13])[CH:5]=1)[CH3:2]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
A mixture of 4-ethoxypyridine 1-oxide (20 g, 144 mmol) in Ac2O (200 mL, 7.836 mol) was heated to refluxed for 4 h. Then, the solvent was removed in vacuo, and the residue was dissolved in MeOH (50 mL) and water (50 mL) and stirred at 25° C. for 16 h. The mixture was then concentrated and the crude material was purified by silica column chromatography (DCM/MeOH=10:1). All fractions found to contain product by TLC (DCM/MeOH=10:1, Rf=0.6) were combined and concentrated to yield a dark yellow solid of 4-ethoxypyridin-2-ol (17 g, 104 mmol, 72% yield). 1H NMR (400 MHz, MeOH-d4) δ 8.20 (d, J=7.6 Hz, 2H), 7.12 (d, J=7.6 Hz, 2H), 4.18 (q, J=7.2 Hz, 2H), 1.42 (t, J=6.8 Hz, 3H); ES-LCMS m/z: 140.0 (M+H).
Aufarbeitung
- temperaturewas heated
- temperatureto refluxed for 4 h
- customThen, the solvent was removed in vacuo
- dissolutionthe residue was dissolved in MeOH (50 mL)
- concentrationThe mixture was then concentrated
- customthe crude material was purified by silica column chromatography (DCM/MeOH=10:1)
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-9987eea31ef4421fb8741ebdaec8e82b
- Quelldatensatz
- uspto-grants-2016_07
- Patentnummer
- US09382238B2
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