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HRID 1030736Erstellt: 25. Oktober 2026
2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone → 4-(Methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/1030736
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone | HCID 11099372 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-(Methoxymethoxy)benzaldehyde | HCID 250074 | 100,1% |
Reaktionsschritte
In 30 ml of methanol were dissolved 14.73 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl-2-butenyl)acetophenone obtained in Production Example 13 and 7.55 g of the p-methoxymethoxybenzaldehyde obtained in Production Example 25, and a saturated solution of sodium hydroxide in methanol was added to the solution and the mixture was stirred at room temperature for 1 day to effect a reaction. After the reaction, the reaction mixture was carefully neutralized with dilute hydrochloric acid and extracted with 1.5 l of ethyl acetate, and the ethyl acetate layer was washed with water (500 ml×4 times), shaken with a saturated aqueous solution of sodium chloride (300 ml×2 times), dried with anhydrous sodium sulfate and filtered. The solvent was removed from the filtrate by distillation to obtain 18.94 g (yield=88.2%) of 2'-hydroxy-4,4',6'-tris(methoxymethoxy)-3'-(3-methyl-2-butenyl)chalcone in the form of a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05106871 |
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| Quelldatensatz | uspto-grants-1992_04 |
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| ORD ID | ord-9cc7bd3ea8fa447caaca978128feddea |
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| Quellennotiz | uspto-grants-1992_04 |
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