반응 #3784

ord-24790d511c784f0cb5c8390c2b1741e2

반응 방정식

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
수율 98.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to react for 6 hours under refluxing conditions
  2. 2
    기타After the completion of the reaction
  3. 3
    세척the chloroform layer was washed with an aqueous solution of sodium bicarbonate
  4. 4
    기타the chloroform was removed under reduced pressures
  5. 5
    기타The reaction product was purified by silicagel column chromatogram

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05734065uspto-grants-1998_03