Reaktion #3784

ord-24790d511c784f0cb5c8390c2b1741e2

Reaktionsgleichung

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
Ausbeute 98.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto react for 6 hours under refluxing conditions
  2. 2
    SonstigeAfter the completion of the reaction
  3. 3
    Waschenthe chloroform layer was washed with an aqueous solution of sodium bicarbonate
  4. 4
    Sonstigethe chloroform was removed under reduced pressures
  5. 5
    SonstigeThe reaction product was purified by silicagel column chromatogram

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05734065uspto-grants-1998_03