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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359199생성일: 2026년 10월 23일

Pyridine → 2'-Methoxymethoxy-3,4-dimethoxy-2-methoxymethoxybenzophenone

https://huagongshe.com/ko/reaction/359199

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물MAGNESIUM SILICATE (synthetic)HCID 61680—
반응물Trioxobis(pyridine)chromiumHCID 88565—
반응물(2-Methoxymethoxyphenyl)(3,4-dimethoxy-2-methoxymethoxyphenyl)methanolHCID 19812677—
촉매chromium (VI) trioxideHCID 10219390—
용매DichloromethaneHCID 6344—
생성물2'-Methoxymethoxy-3,4-dimethoxy-2-methoxymethoxybenzophenoneHCID 19812692—

반응 단계

A mixture 12.3 g (126 mmol) of chromium trioxide in 153 ml of dichloromethane was cooled to 0° C. and 20.3 ml (252 mmol) of pyridine were added with stirring to obtain, after 45 min, a yellow-brown solution (Collin's reagent). (2-Methoxymethoxyphenyl)(3,4-dimethoxy-2-methoxymethoxyphenyl)methanol (7.67 g, 21 mmol) was added with stirring and the mixture allowed to warm to room temperature with stirring overnight. Twenty grams of florisil were added and the mixture was concentrated by evaporation under reduced pressure and filtered through celite and then further eluted with ether. The resulting mixture was concentrated under reduced pressure and purified by liquid chromatography using a Waters Prep 500 Chromatograph with a silica gel column and eluting with a 70:30 mixture of hexane and ethyl acetate to obtain 6.0 g (79 percent of theory) of the title compound as an oil. The proton and carbon NMR and infrared spectra were consistent with the assigned structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999448
출처 데이터셋uspto-grants-1991_03
ORD IDord-6551b7ee262c411d894b73a2e53c812e
출처 메모uspto-grants-1991_03