HCID 14078470, Verbindung → 4-Methoxybenzaldehyde

HRID 2254252Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2254252
O[C:2]1[C:7](CC=C(C)C)=[C:6]([O:13][CH3:14])[CH:5]=[CH:4][C:3]=1[C:15](=[O:17])C>C(O)C>[CH:15](=[O:17])[C:3]1[CH:2]=[CH:7][C:6]([O:13][CH3:14])=[CH:5][CH:4]=1

Komponenten

3

Versuchsvorschrift

In 5 ml of ethanol were dissolved 0.48 g of 2'-hydroxy-4'-methoxy-3'-(3-methyl-2-butenyl)acetophenone obtained in production Example 9 and 0.35 ml of p-anisaldehyde. The solution was cooled to 0° C. and 7.5 ml of a saturated ethanol solution of potassium hydroxide was added to the solution, and the mixture was stirred at 0° C. for 30 minutes and at room temperature for 4 days. After the reaction, 3 N hydrochloric acid was added to the reaction liquid under cooling to gradually make the liquid acidic, and the formed precipitate was recovered by filtration and recrystallized from methanol to obtain 0.47 g (yield=64.7%) of 2'-hydroxy-4,4'-dimethoxy-3'-(3-methyl-2-butenyl)chalcone in the form of a yellow needle.

Quellen und Nachweise

ORD-Eintrag
ord-9a5be756af3949c1904be89796d2f6e3
Quelldatensatz
uspto-grants-1993_08
Patentnummer
US05234951

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