反応 #3784

ord-24790d511c784f0cb5c8390c2b1741e2

反応方程式

Cc1sc([Si](C)(C)C)cc1C1=C(c2cc([Si](C)(C)C)sc2C)C(F)(F)C(F)(F)C1(F)F
1,2-bis(2-methyl-5-trimethylsilyl-3-thienyl)hexafluorocyclopentene
Br
hydrobromic acid
Cc1sccc1C1=C(c2ccsc2C)C(F)(F)C(F)(F)C1(F)F
1,2-bis(2-methyl-3-thienyl)hexafluorocyclopentene
収率 98.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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).

出典

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