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HRID 1030763作成日:2026年10月25日
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/1030763
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone | HCID 11099372 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(Methoxymethoxy)-3-(3-methylbut-2-en-1-yl)benzaldehyde | HCID 14559752 | — |
反応手順
In 45 ml of ethanol were dissolved 6.99 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-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 6N 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-2-butenyl)chalcone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05106871 |
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| 出典データセット | uspto-grants-1992_04 |
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| ORD ID | ord-4dba58bd42d3462d8a7eec80dc55772c |
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| 出典メモ | uspto-grants-1992_04 |
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