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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2254205생성일: 2026년 10월 26일

2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone → 2'-Hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenone

https://huagongshe.com/reaction/2254205

반응식

참여 물질

역할이름HCID투입량
반응물2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
반응물HCID 178418361HCID 178418361—
용매EthanolHCID 702—
생성물2'-Hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenoneHCID 1609453182.8%

반응 단계

A solution of 2.08 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl-2-butenyl)acetophenone obtained in Production Example 13 in ethanol (20 ml) was added to a sufficiently hydrogen gas-absorbed suspension of 1.0 g of 5% palladium-carbon in 30 ml of ethanol, and the mixture was stirred at room temperature under atmospheric pressure in a hydrogen atmosphere. After the reaction, the reaction mixture was filtered, and the solvent was removed from the filtrate by distillation. The obtained residue was subjected to the silica gel column chromatography (3.0 cm in diameter, 60 g of silica gel, 0.3 kg/cm2) using a mixed solvent of n-hexane and ethyl acetate (n-hexane/ethyl acetate-3/1). Fractions of 50 ml were recovered, and 1.73 g (yield=82.8%) of 2'-hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenone in the form of a yellow oil was obtained from the third to fifth fractions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05234951
출처 데이터셋uspto-grants-1993_08
ORD IDord-647ea5649e784bf594788f2ea2fee9e0
출처 메모uspto-grants-1993_08