Reaktion #955958

ord-9d6dedd5906e404490d11b8f63788366

Reaktionsgleichung

CCCCC(C#Cc1c2ccsc2c(C#CC(CC)CCCC)c2ccsc12)CC
4,8-bis(3-ethylhept-1-ynyl)thieno[2,3-f]benzothiophene
CCCCC(CC)CCc1c2ccsc2c(CCC(CC)CCCC)c2ccsc12
oil
Ausbeute 54.0%
CCCCC(CC)CCc1c2ccsc2c(CCC(CC)CCCC)c2ccsc12
4,8-bis(3-ethylheptyl)thieno[2,3-f]benzothiophene
Ausbeute 54.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA dry 250 mL 1-neck flask was flushed with N2
  2. 2
    SonstigeThe flask was evacuated
  3. 3
    Filtrationthe mixture was filtered through Celite and solvent
  4. 4
    Sonstigewas removed by rotary evaporation
  5. 5
    workup.DISSOLUTIONThe solid was dissolved in hexanes
  6. 6
    Sonstigepurified by column chromatography

Vorschrift

A dry 250 mL 1-neck flask was flushed with N2 and was charged with 4,8-bis(3-ethylhept-1-ynyl)thieno[2,3-f]benzothiophene (3.04 g, 0.007 mol), Pd/C wet support (0.82 g, 10%) and THF (15 mL, 0.5 M). The flask was evacuated and backfilled with hydrogen. The flask was kept under a hydrogen atmosphere and was monitored by TLC. After the reaction was completed, the mixture was filtered through Celite and solvent was removed by rotary evaporation. The solid was dissolved in hexanes and purified by column chromatography to yield oil (1.66 g, 54%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968885B2uspto-grants-2015_03