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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2254278Erstellt: 27. Oktober 2026

2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone → 4-(Methoxymethoxy)-3-(3-methylbut-2-en-1-yl)benzaldehyde

https://huagongshe.com/reaction/2254278

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
LösungsmittelEthanolHCID 702—
Produkt4-(Methoxymethoxy)-3-(3-methylbut-2-en-1-yl)benzaldehydeHCID 14559752—

Reaktionsschritte

In 45 ml of ethanol were dissolved 6.99 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl- 2-butenyl)acetophenone obtained in Production Example 13 and 5.01 of the 4-methoxymethoxy-3-(3-methyl-2-butenyl)benzaldehyde, and the solution was cooled to 0° C. Then, 65 ml of a saturated solution of potassium hydroxide in ethanol was added to the solution and the mixture was stirred at room temperature overnight. The reaction liquid was neutralized with 6 N hydrochloric acid and extracted with ethyl acetate, and the ethyl acetate layer was washed with water, dried with anhydrous sodium sulfate and filtered. The solvent was removed from the filtrate by distillation and the residue was recrystallized from n-hexane to obtain 7.22 g (yield=61.7%) of 2'-hydroxy-4,4',6'-tris(methoxymethoxy)-3,3'-bis(3-methyl-2butenyl)chalcone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05234951
Quelldatensatzuspto-grants-1993_08
ORD IDord-e951c54df41e4d16a535c70181c50693
Quellennotizuspto-grants-1993_08