反应 #1398
ord-d880e525dd19411dbb94deface4386f9
反应方程式
反应条件
后处理
- 1其他To a 250 mL round bottomed flask equipped with a heating mantle, overhead agitator
- 2workup.ADDITIONthermometer, condenser, and addition funnel with a tube protruding below the liquid level
- 3洗涤to wash the MnO2 beaker
- 4workup.ADDITIONwere added to the flask
- 5其他to reach about 100° C. at which
- 6workup.ADDITIONwere added to the addition funnel
- 7其他slowly rose to about 125° C.
- 8workup.ADDITIONhad been added
- 9温度The mixture was heated
- 10其他after approximately 12 hours
- 11温度to cool to 100° C.
- 12其他fitted with No
- 13过滤42 filter paper
- 14其他to form a filter pre-coat
- 15过滤vacuum filtered
- 16洗涤to wash the flask
- 17洗涤The filter cake was then washed with 100 g toluene
- 18温度heated to about 50° to 70° C.
- 19其他the filtrate phase separated
- 20其他The toluene was removed from the organic phase
- 21温度by heating to approximately 65° C. at 10 mm Hg
- 22其他The solids were recrystallized from a hexane solvent
实验过程
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.