反应 #63590

ord-1154f6862b354bcc8357c14211d3a48c

反应方程式

Cl
hydrochloric acid
[Al+3].[Cl-].[Cl-].[Cl-]
aluminium chloride
Fc1ccccc1
fluorobenzene
O=C1CCC(O)(c2ccc(F)cc2)CC1
4-(4-fluorophenyl)-4-hydroxycyclohexanone
O=C1CCC(c2ccc(F)cc2)(c2ccc(F)cc2)CC1
4,4-bis(4-fluorophenyl)-1-cyclohexanone
收率 75.9%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled
  2. 2
    workup.STIRRINGUpon completion, stirring
  3. 3
    温度while still cooling
  4. 4
    workup.ADDITIONby pouring onto a mixture of crushed ice
  5. 5
    萃取The product was extracted with methylbenzene
  6. 6
    洗涤The extract was washed with water till neutralization,
  7. 7
    其他dried
  8. 8
    过滤filtered
  9. 9
    其他evaporated
  10. 10
    其他The residue was purified by column-chromatography over silica gel
  11. 11
    其他The pure fractions were collected
  12. 12
    其他the eluent was evaporated

实验过程

To a stirred and cooled (ice-bath) mixture of 50 parts of fluorobenzene and 4.1 parts of 4-(4-fluorophenyl)-4-hydroxycyclohexanone were added portionwise 11 parts of aluminium chloride. Upon completion, stirring was continued for 2 hours while still cooling. The reaction mixture was decomposed by pouring onto a mixture of crushed ice and a hydrochloric acid solution. The product was extracted with methylbenzene. The extract was washed with water till neutralization, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated, yielding 4.3 parts (75.9%) of 4,4-bis(4-fluorophenyl)-1-cyclohexanone as a residue (intermediate 19).

来源

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