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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

反応式

関与物質

役割名称HCID仕込み量
反応物2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
溶媒EthanolHCID 702—
生成物4-(Methoxymethoxy)-3-(3-methylbut-2-en-1-yl)benzaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05106871
出典データセットuspto-grants-1992_04
ORD IDord-4dba58bd42d3462d8a7eec80dc55772c
出典メモuspto-grants-1992_04