反应 #3784

ord-24790d511c784f0cb5c8390c2b1741e2

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to react for 6 hours under refluxing conditions
  2. 2
    其他After the completion of the reaction
  3. 3
    洗涤the chloroform layer was washed with an aqueous solution of sodium bicarbonate
  4. 4
    其他the chloroform was removed under reduced pressures
  5. 5
    其他The reaction product was purified by silicagel column chromatogram

实验过程

1,2-bis(2-methyl-5-trimethylsilyl-3-thienyl)hexafluorocyclopentene (2.16 g, 0.005 mol) was dissolved in chloroform (200 ml) and was allowed to react for 6 hours under refluxing conditions by adding concentrated hydrobromic acid (10 ml) to the solution. After the completion of the reaction, the chloroform layer was washed with an aqueous solution of sodium bicarbonate and the chloroform was removed under reduced pressures. The reaction product was purified by silicagel column chromatogram to give 1,2-bis(2-methyl-3-thienyl)hexafluorocyclopentene (1.8 g, 0.0049 mol).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05734065uspto-grants-1998_03