Reaktionsgleichung
[O:1]=[C:2]([CH2:9][CH3:10])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH2:11](O)[CH2:12][OH:13].C(OCC)(OCC)OCC.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C(OCC)(=O)C.CCCCCCC>[CH2:7]([O:6][C:4](=[O:5])[CH2:3][C:2]1([CH2:9][CH3:10])[O:13][CH2:12][CH2:11][O:1]1)[CH3:8]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of ethyl 3-oxopentanoate (5 g, 34.7 mmol), ethylene glycol (10.8 g, 174 mmol), triethyl orthoformate (5.14 g, 34.7 mmol), and p-toluenesulfonic acid monohydrate (598 mg, 3.14 mmol) was stirred at room temperature overnight. To the reaction mixture, heptane and ethyl acetate were added to dilute solution, which was washed with water. The organic layer was washed with a saturated saline solution, dried over magnesium sulfate, filtrated and the filtrate was concentrated under reduced pressure. The residue was dissolved in heptane and subjected to NH silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=1/0→10/1) to obtain the title compound (3.85 g, yield: 58.9%) as colorless oil.
Aufarbeitung
- washwas washed with water
- washThe organic layer was washed with a saturated saline solution
- dry with materialdried over magnesium sulfate
- filtrationfiltrated
- concentrationthe filtrate was concentrated under reduced pressure
- dissolutionThe residue was dissolved in heptane
- washsubjected to NH silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=1/0→10/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-0f477811c9694e35a09ec124018f0987
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07425634B2
Verknüpfte Notizen
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