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HRID 1030736作成日:2026年10月27日
2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone → 4-(Methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/1030736
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 | Methanol | HCID 887 | — |
| 生成物 | 4-(Methoxymethoxy)benzaldehyde | HCID 250074 | 100.1% |
反応手順
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.
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-9cc7bd3ea8fa447caaca978128feddea |
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| 出典メモ | uspto-grants-1992_04 |
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