Ethanol → 5-ethoxy-2-methyl-2H-pyran-3(6H)-one
Reaktionsgleichung
[CH3:1][CH:2]1[C:7](=[O:8])[CH2:6][C:5](=[O:9])[CH2:4][O:3]1.[CH2:10](O)[CH3:11]>S(=O)(=O)(O)O>[CH2:10]([O:9][C:5]1[CH2:4][O:3][CH:2]([CH3:1])[C:7](=[O:8])[CH:6]=1)[CH3:11]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The product from Example 84C (3.0 g, 23 mmol) was dissolved in ethanol (50 mL), treated with concentrated sulfuric acid (5 drops), heated to reflux for 3 hours and concentrated. The residue was purified by chromatography eluting with 10:1 and then 5:1 and then 2:1 hexane:ethyl acetate to provide the title compound as the faster moving isomer.
Aufarbeitung
- temperatureheated
- temperatureto reflux for 3 hours
- concentrationconcentrated
- customThe residue was purified by chromatography
- washeluting with 10:1
Quellen und Nachweise
- ORD-Eintrag
- ord-13a9e2ec99674901be2c87a3f05fe087
- Quelldatensatz
- uspto-grants-2003_11
- Patentnummer
- US06642222B2
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