Reaktionsgleichung
O[C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4](OC)[C:3]=1[C:12](=[O:14])C.C(O)C>CS(C)=O>[CH:12](=[O:14])[C:3]1[CH:2]=[CH:7][C:6]([O:8][CH3:9])=[CH:5][CH:4]=1Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a mixture of 34.7 g of the 2'-hydroxy-4',6'-dimethoxyacetophenone obtained in Production Example 7, 25.3 g of p-anisaldehyde, 150 ml of ethanol and 150 ml of dimethylsulfoxide was added 150 ml of a saturated solution of potassium hydroxide in ethanol at 0° C., and the mixture was stirred at room temperature for 4 hours to effect reaction. After the reaction, the reaction mixture was made acidic by dilute hydrochloric acid to obtain a precipitate. The precipitate was washed with water and recrystallized from a mixed solvent of methanol and ethyl acetate to obtain 43.4 g (yield=78.4%) of 2'-hydroxy-4,4',6'-trimethoxychalcone in the form of a yellow needle.
Quellen und Nachweise
- ORD-Eintrag
- ord-35fe829a988b43b4bc56271c95117966
- Quelldatensatz
- uspto-grants-1992_04
- Patentnummer
- US05106871
Verknüpfte Notizen
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