反应 #955958

ord-9d6dedd5906e404490d11b8f63788366

反应方程式

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
收率 54.0%
CCCCC(CC)CCc1c2ccsc2c(CCC(CC)CCCC)c2ccsc12
4,8-bis(3-ethylheptyl)thieno[2,3-f]benzothiophene
收率 54.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他A dry 250 mL 1-neck flask was flushed with N2
  2. 2
    其他The flask was evacuated
  3. 3
    过滤the mixture was filtered through Celite and solvent
  4. 4
    其他was removed by rotary evaporation
  5. 5
    workup.DISSOLUTIONThe solid was dissolved in hexanes
  6. 6
    其他purified by column chromatography

实验过程

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%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08968885B2uspto-grants-2015_03