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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1302Erstellt: 23. Oktober 2026

Sulfuric Acid → 4,4'-Difluorobenzophenone

https://huagongshe.com/de/reaction/1302

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTolueneHCID 1140—
Edukt1,1'-Methylenebis[4-fluorobenzene]HCID 96094—
KatalysatorManganese dioxideHCID 14801—
LösungsmittelWaterHCID 962—
Produkt4,4'-DifluorobenzophenoneHCID 958269,2%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

To a 250 mL round bottomed flask equipped with a heating mantle, overhead agitator, thermometer, condenser, and addition funnel with a tube protruding below the liquid level was added 10.6 g 4,4'-difluorodiphenylmethane (0.051 moles). Agitation was begun and a slurry of 20.5 g MnO2 (0.195 moles) in 30 g water was added to the flask. About 30 g of water were used to wash the MnO2 beaker and were added to the flask. The mixture was allowed to reach about 100° C. at which point 50 g H2SO4 (0.487 moles) were added to the addition funnel. The H2SO4 was then added dropwise into the flask and the reaction temperature slowly rose to about 125° C. when all of the acid had been added. The mixture was heated to maintain the temperature at about 125° C. until gas chromatography showed complete conversion after approximately 12 hours. The reaction mixture was allowed to cool to 100° C. and 50 g toluene were added to the mixture. A slurry of 6 g diatomaceous earth in 30 g water was poured into a vacuum Buchner funnel fitted with No. 42 filter paper to form a filter pre-coat. The contents of the round bottomed flask were then vacuum filtered. 10 g toluene was used to wash the flask and, subsequently, the filter cake. The filter cake was then washed with 100 g toluene heated to about 50° to 70° C. and the filtrate phase separated. The toluene was removed from the organic phase by heating to approximately 65° C. at 10 mm Hg. The 10 g yellow solids assayed as 95% pure 4,4'-difluorobenzophenone for an 84% yield. The solids were recrystallized from a hexane solvent leaving 7.7 g crystalline 4,4'-difluorobenzophenone for a 68% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723676
Quelldatensatzuspto-grants-1998_03
ORD IDord-d880e525dd19411dbb94deface4386f9
Quellennotizuspto-grants-1998_03