反应 #1727228

ord-1d63c04f9c5849b38c9c3d181b6e7f0d

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas charged into an argon-
  2. 2
    workup.ADDITIONfilled 200 mL flask
  3. 3
    其他fitted with a condenser
  4. 4
    温度The mixture was heated
  5. 5
    温度under reflux in an argon atmosphere for 24 h
  6. 6
    过滤filtered
  7. 7
    workup.ADDITION50 mL of 2N HCl was added dropwise
  8. 8
    workup.STIRRINGthe mixture was stirred for 30 min
  9. 9
    其他The yellow suspension was decanted
  10. 10
    过滤filtered
  11. 11
    其他to give a yellow solid
  12. 12
    过滤filtered
  13. 13
    洗涤The solid was washed with deionized water, methanol
  14. 14
    其他dried

实验过程

A mixture of 5,11-dihydridoindolo[3,2-b]carbazole (2.56 g, 10 mmol), 18-crown-6 (0.52 g, 2.0 mmol), K2CO3 (11.06 g, 80 mmol), 4-iodotoluene (6.54 g, 30 mmol), copper (2.54 g, 40 mmol), and 1,2-dichlorobenzene (40 mL) was charged into an argon-filled 200 mL flask fitted with a condenser. The mixture was heated under reflux in an argon atmosphere for 24 h. Subsequently, the reaction mixture was cooled down to room temperature, diluted with toluene, and filtered. The solid was stirred in 50 mL of N,N-dimethylformamide and 50 mL of 2N HCl was added dropwise and the mixture was stirred for 30 min. The yellow suspension was decanted and filtered to give a yellow solid. The solid was then stirred in a mixture of DMSO (200 mL) and 20% NaOH (50 mL) for 30 min and then filtered. The solid was washed with deionized water, methanol, and dried to yield 1.65 g of 5,11-bis(4-methylphenyl)indolo[3,2-b]carbazole, which was then subject to train sublimation to obtain electrically pure compound for OTFT fabrication. DSC showed two endotherms at 305° C. and 322° C. on first heating. 1H NMR (CDCl3): δ 8.11 (d, J=7.8 Hz, 2H), 8.04 (s, 2H), 7.57 (d, J=8.3 Hz, 4H), 7.48 (d, J=8.3 Hz, 4H), 7.39 (d, J=3.7 Hz, 4H), 7.21 (m, 2H), 2.54 (s, 6H); IR (NaCl): 3034, 2916, 1606, 1515, 1451, 1323, 1235, 1191, 819, 741 cm−1.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08110690B2uspto-grants-2012_02