Cesium carbonate → HCID 22026619, 화합물

HRID 1434895

반응식

HRID 1434895 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[NH:8][CH:9]=[CH:10][N:11]=1.I[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C.[Cu]>[C:13]1([N:11]2[CH:10]=[CH:9][N:8]=[C:7]2[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

6

실험 절차

2-(2-pyridyl)imidazole (6.91 g), iodobenzene (11.47 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.

후처리

  1. customequipped with a magnetic stirrer and a reflux condenser
  2. customThe mixture is degassed with N2 for 15 minutes at room temperature
  3. temperaturerefluxed under N2 in an oil bath for 24 hours
  4. filtrationsuction-filtered
  5. customto remove the solid byproduct
  6. extractionThe filtrate was extracted with EtOAc (3×100 mL)
  7. washThe combined organic layer was washed with H2O (2×100 mL)
  8. dry with materialwith saturated NaCl (2×150 mL), and subsequently dried with anhydrous Na2SO4
  9. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-da48b5caef14449797818581e2fb8952
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07615637B2

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