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HRID 466936作成日:2026年10月26日

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

https://huagongshe.com/reaction/466936

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物MAGNESIUM SILICATE (synthetic)HCID 61680—
反応物Trioxobis(pyridine)chromiumHCID 88565—
反応物(2-Methoxymethoxyphenyl)(3,4-dimethoxy-2-methoxymethoxyphenyl)methanolHCID 19812677—
触媒chromium (VI) trioxideHCID 10219390—
溶媒DichloromethaneHCID 6344—
生成物2'-Methoxymethoxy-3,4-dimethoxy-2-methoxymethoxybenzophenoneHCID 19812692—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05158597
出典データセットuspto-grants-1992_10
ORD IDord-9b906bc85dea4257a97f75d18bccc2c9
出典メモuspto-grants-1992_10