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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2254278생성일: 2026년 10월 27일

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/2254278

반응식

참여 물질

역할이름HCID투입량
반응물2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
용매EthanolHCID 702—
생성물4-(Methoxymethoxy)-3-(3-methylbut-2-en-1-yl)benzaldehydeHCID 14559752—

반응 단계

In 45 ml of ethanol were dissolved 6.99 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl- 2-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 6 N 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-2butenyl)chalcone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05234951
출처 데이터셋uspto-grants-1993_08
ORD IDord-e951c54df41e4d16a535c70181c50693
출처 메모uspto-grants-1993_08