تفاعل #1398

ord-d880e525dd19411dbb94deface4386f9

معادلة التفاعل

Fc1ccc(Cc2ccc(F)cc2)cc1
4,4'-difluorodiphenylmethane
O=S(=O)(O)O
H2SO4
Cc1ccccc1
toluene
O=S(=O)(O)O
H2SO4
O=C(c1ccc(F)cc1)c1ccc(F)cc1
4,4'-difluorobenzophenone
المردود 69.2%

الكواشف

المذيبات

ظروف التفاعل

درجة الحرارة
125°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 250 mL round bottomed flask equipped with a heating mantle, overhead agitator
  2. 2
    workup.ADDITIONthermometer, condenser, and addition funnel with a tube protruding below the liquid level
  3. 3
    غسيلto wash the MnO2 beaker
  4. 4
    workup.ADDITIONwere added to the flask
  5. 5
    أخرىto reach about 100° C. at which
  6. 6
    workup.ADDITIONwere added to the addition funnel
  7. 7
    أخرىslowly rose to about 125° C.
  8. 8
    workup.ADDITIONhad been added
  9. 9
    درجة الحرارةThe mixture was heated
  10. 10
    أخرىafter approximately 12 hours
  11. 11
    درجة الحرارةto cool to 100° C.
  12. 12
    أخرىfitted with No
  13. 13
    ترشيح42 filter paper
  14. 14
    أخرىto form a filter pre-coat
  15. 15
    ترشيحvacuum filtered
  16. 16
    غسيلto wash the flask
  17. 17
    غسيلThe filter cake was then washed with 100 g toluene
  18. 18
    درجة الحرارةheated to about 50° to 70° C.
  19. 19
    أخرىthe filtrate phase separated
  20. 20
    أخرىThe toluene was removed from the organic phase
  21. 21
    درجة الحرارةby heating to approximately 65° C. at 10 mm Hg
  22. 22
    أخرىThe solids were recrystallized from a hexane solvent

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723676uspto-grants-1998_03