反应 #63578

ord-a1cb8412e9314137a5c53588cbedab76

反应方程式

Cl
hydrochloric acid
[Al+3].[Cl-].[Cl-].[Cl-]
aluminium chloride
O=C1OC(=O)c2ccccc21
1,3-isobenzofurandione
Fc1ccccc1
fluorobenzene
O=C(O)c1ccccc1C(=O)c1ccc(F)cc1
2-(4-fluorobenzoyl)benzoic acid
收率 80.7%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度Upon completion, the whole was heated slowly
  2. 2
    温度to reflux
  3. 3
    温度at reflux temperature
  4. 4
    温度The reaction mixture was cooled
  5. 5
    萃取The product was extracted twice with dichloromethane
  6. 6
    洗涤The combined extracts were washed with a sodium hydroxide solution 10%
  7. 7
    其他The aqueous phase was separated
  8. 8
    洗涤washed with 2,2'-oxybispropane
  9. 9
    温度while cooling
  10. 10
    workup.STIRRINGThe whole was stirred for one hour at room temperature
  11. 11
    过滤The precipitated product was filtered off
  12. 12
    workup.DISSOLUTIONdissolved in benzene
  13. 13
    workup.DISTILLATIONThe solution was distilled azeotropically
  14. 14
    其他to dry
  15. 15
    workup.STIRRINGThe solid residue was stirred in hexane
  16. 16
    过滤The product was filtered off
  17. 17
    其他dried in vacuo at about 50° C.

实验过程

To a stirred mixture of 25 parts of 1,3-isobenzofurandione and 108.5 parts of fluorobenzene were added portionwise 50 parts of aluminium chloride. Upon completion, the whole was heated slowly to reflux and stirring was continued for 1.50 hours at reflux temperature. The reaction mixture was cooled and poured onto a mixture of crushed ice and 60 parts of concentrated hydrochloric acid. The product was extracted twice with dichloromethane. The combined extracts were washed with a sodium hydroxide solution 10%. The aqueous phase was separated, washed with 2,2'-oxybispropane and acidified with concentrated hydrochloric acid while cooling. The whole was stirred for one hour at room temperature. The precipitated product was filtered off and dissolved in benzene. The solution was distilled azeotropically to dry. The solid residue was stirred in hexane. The product was filtered off and dried in vacuo at about 50° C., yielding 33.5 parts (80.7%) of 2-(4-fluorobenzoyl)benzoic acid; mp. 129.2° C. (intermediate 7).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04766125uspto-grants-1988_08