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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26374Erstellt: 24. Oktober 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-Hydroxy-7-methoxy-5-benzofurancarboxaldehyde

https://huagongshe.com/de/reaction/26374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Edukt2,3-Dihydro-6-hydroxy-7-methoxy-5-benzofurancarboxaldehydeHCID 21856572—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-Hydroxy-7-methoxy-5-benzofurancarboxaldehydeHCID 21785684—

Reaktionsschritte

A solution of 817 mg. (3.6 mmole) of DDQ in 10 ml. of dioxane was added to 582 mg. (3 mmole) of 2,3-dihydro-6-hydroxy-7-methoxy-5-benzofuran-carboxaldehyde in 15 ml. of dioxane and the resulting mixture was heated under reflux for 7 hours, cooled and the formed solid removed by filtration. The precipitate was thoroughly washed first with benzene, then with CHCl3. The washings were combined with the initial filtrate and the total concentrated in vacuo to a residue which was chromatographed first on a 20 ml. dry silica gel column (E. Merck 7734) with CHCl3 elution followed by conventional chromatography over 20 g. of silica (E. Merck 7734) packed in benzene-ethyl acetate (95:5) and elution with this solvent mixture provided, after workup, a yellow solid, m.p. 60°-62°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04150042
Quelldatensatzuspto-grants-1979_04
ORD IDord-faaced70dcaa4b2b8d73c3c300f64d98
Quellennotizuspto-grants-1979_04