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

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.

1. customto obtain, after 45 min
2. stirringwith stirring
3. stirringwith stirring overnight
4. concentrationthe mixture was concentrated by evaporation under reduced pressure
5. filtrationfiltered through celite
6. washfurther eluted with ether
7. concentrationThe resulting mixture was concentrated under reduced pressure
8. custompurified by liquid chromatography
9. washeluting with a 70:30 mixture of hexane and ethyl acetate

ORD-Eintrag

ord-9b906bc85dea4257a97f75d18bccc2c9

Quelldatensatz

uspto-grants-1992_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05158597