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HRID 1792973생성일: 2026년 10월 27일

Imidazole → 1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanone

https://huagongshe.com/reaction/1792973

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물AcetosyringoneHCID 17198—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매DimethylformamideHCID 6228—
생성물1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanoneHCID 2202559381%

반응 단계

Ex-59A: To a solution of 4′-hydroxy-3′,5′-dimethoxyacetophenone (1 g, 5.1 mmol) in N,N-dimethylformamide were added tert-butyldimethylsilyl chloride (1,15 g, 7.6 mmol) and imidazole (0.69 g, 10.2 mmol). The mixture was stirred at room temperature overnight. Upon quenching with 1 M sulfuric acid solution, the mixture was extracted with dichloromethane. The organic phase was washed with saturated sodium bicarbonate and brine. It was dried and evaporated. Water (2 mL) was added to the residue, and the precipitate was filtered out and dried over an oil pump to give 1.28 g (81%) of 3′,5′-dimethoxy-4′-(tert-butyldimethylsiloxy)acetophenone as a white solid, m.p. 90-92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07078431B2
출처 데이터셋uspto-grants-2006_07
ORD IDord-2095895f6d47499b941b0e13f624eeae
출처 메모uspto-grants-2006_07