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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131660Erstellt: 26. Oktober 2026

Acetaldehyde, 2,2-dimethoxy- → 3-(4,7-Dihydroxy-5-methyl-2-oxo-2H-chromene-3-yl)-7-hydroxy-9-methyl-2-methoxy-2,3-dihydro-4H-furo[3.2-c]chromene-4-one

https://huagongshe.com/reaction/131660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehyde, 2,2-dimethoxy-HCID 162650—
Edukt4,7-Dihydroxy-5-methylcoumarinHCID 54707775—
LösungsmittelMethanolHCID 887—
Produkt3-(4,7-Dihydroxy-5-methyl-2-oxo-2H-chromene-3-yl)-7-hydroxy-9-methyl-2-methoxy-2,3-dihydro-4H-furo[3.2-c]chromene-4-oneHCID 8676068992%

Reaktionsschritte

4,7-Dihydroxy-5-methylcoumarin (200 mg; 1.04 mmole) was dissolved in methanol (5 mL). A 60% aqueous dimethoxyacetaldehyde solution (792 μL; 8.7 mmole) was added and the reaction mixture was refluxed for 5 hours. By cooling to room temperature a white precipitate was precipitated, which was filtered off and washed with methanol. Obtained was the title compound in a 92% yield and of sufficient purity to be used in the next synthesis step:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384975B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-95b24f291c7d40b5b049ff1f6c9402c9
Quellennotizuspto-grants-2008_06