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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359199Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktMAGNESIUM SILICATE (synthetic)HCID 61680—
EduktTrioxobis(pyridine)chromiumHCID 88565—
Edukt(2-Methoxymethoxyphenyl)(3,4-dimethoxy-2-methoxymethoxyphenyl)methanolHCID 19812677—
Katalysatorchromium (VI) trioxideHCID 10219390—
LösungsmittelDichloromethaneHCID 6344—
Produkt2'-Methoxymethoxy-3,4-dimethoxy-2-methoxymethoxybenzophenoneHCID 19812692—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04999448
Quelldatensatzuspto-grants-1991_03
ORD IDord-6551b7ee262c411d894b73a2e53c812e
Quellennotizuspto-grants-1991_03