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HRID 1030699作成日:2026年10月26日

Ethanol → 3-Methoxy-4-(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/1030699

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
生成物3-Methoxy-4-(methoxymethoxy)benzaldehydeHCID 79661—

反応手順

In 95.0 ml of ethanol were dissolved 14.8 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl-2-butenyl)acetophenone obtained in Production Example 1 and 9.0 g of the 3-methoxy-4-methoxymethoxybenzaldehyde obtained in Production Example 17, the solution was cooled to 0° C., and 138.0 ml of a saturated solution of potassium hydroxide in ethanol was added to the solution. The temperature was elevated to room temperature and the reaction liquid was stirred for 15 hours. The reaction liquid was made acidic by an addition of hydrochloric acid and extracted with diethyl ether. The ether layer was concentrated under a reduced pressure. The reaction mixture was subjected to the column chromatography [230-400 mesh Kieselgel 60; eluting solvent=hexane/ethyl acetate (3/1)] to obtain 13.1 g (yield=57.0%) of 2'-hydroxy-3-methoxy-4,4',6'-tris(methoxymethoxy)-3'-(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-4a674408c9f04e678b6366c3c39eb5dd
出典メモuspto-grants-1992_04