反応 #742263

ord-5e2f1ab688694644a4906b34afdf2afc

反応方程式

c1ccc(-c2ncc[nH]2)nc1
2-(2-pyridyl)imidazole
Ic1ccccc1
iodobenzene
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
c1ccc(-n2ccnc2-c2ccccn2)cc1
1-phenyl-2(2-pyridyl)imidazole

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他equipped with a magnetic stirrer and a reflux condenser
  2. 2
    その他The mixture is degassed with N2 for 15 minutes at room temperature
  3. 3
    温度refluxed under N2 in an oil bath for 24 hours
  4. 4
    ろ過suction-filtered
  5. 5
    その他to remove the solid byproduct
  6. 6
    抽出The filtrate was extracted with EtOAc (3×100 mL)
  7. 7
    洗浄The combined organic layer was washed with H2O (2×100 mL)
  8. 8
    乾燥with saturated NaCl (2×150 mL), and subsequently dried with anhydrous Na2SO4
  9. 9
    その他Evaporation of the solvent

実験手順

2-(2-pyridyl)imidazole (6.91 g), iodobenzene (1.47 g), Cs2CO3 (25 g), and copper powder (15 g) were mixed in 60 mL anhydrous DMF in a 250 mL round bottom flask equipped with a magnetic stirrer and a reflux condenser. The mixture is degassed with N2 for 15 minutes at room temperature and then refluxed under N2 in an oil bath for 24 hours. The resulting mixture was cooled to room temperature and suction-filtered to remove the solid byproduct. The filtrate was extracted with EtOAc (3×100 mL). The combined organic layer was washed with H2O (2×100 mL) and then with saturated NaCl (2×150 mL), and subsequently dried with anhydrous Na2SO4. Evaporation of the solvent gave crude 1-phenyl-2(2-pyridyl)imidazole. The crude product is generally pure enough to use in making redox mediators, although the crude product may be further purified using a silica gel column and eluting with MeOH/CHCl3.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08070934B2uspto-grants-2011_12