反应 #2139924

ord-e3e4ddff55fb4d9fbf83ffd6880dc13d

反应方程式

O=C1C=CC=C2C1=Cc1ccccc12
fluorenone
Brc1ccccc1-c1ccccc1
2-bromobiphenyl
c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21
9.9′-Spirobifluorene
收率 80.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    温度refluxed
  3. 3
    过滤The produced yellow precipitate was filtered
  4. 4
    workup.STIRRINGstirred in cold ammonium chloride
  5. 5
    过滤the obtained crystal was filtered again
  6. 6
    其他dried
  7. 7
    workup.ADDITIONThereafter, acetic acid was added to the solid product
  8. 8
    温度the solution was refluxed
  9. 9
    workup.STIRRINGwhile stirring
  10. 10
    workup.ADDITIONA small amount of hydrochloric acid was added
  11. 11
    其他to obtain the solid target compound
  12. 12
    过滤The solid target compound was filtered
  13. 13
    洗涤washed
  14. 14
    其他to obtain pure target compound with the yield of 80%

实验过程

As shown in the following reaction 1, 6.1 g of 2-bromobiphenyl and 0.585 g of dried Mg were dissolved with ether, and 4.2 g of fluorenone dissolved in ether was added thereto, and refluxed while stirring overnight. The produced yellow precipitate was filtered, and stirred in cold ammonium chloride, and then the obtained crystal was filtered again and dried. Thereafter, acetic acid was added to the solid product, and the solution was refluxed while stirring. A small amount of hydrochloric acid was added thereto to obtain the solid target compound. The solid target compound was filtered and washed to obtain pure target compound with the yield of 80%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07326474B2uspto-grants-2008_02