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Chemical Structure| 928050-07-1 Chemical Structure| 928050-07-1

Structure of 928050-07-1

Chemical Structure| 928050-07-1

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Product Details of [ 928050-07-1 ]

CAS No. :928050-07-1
Formula : C30H20BrN
M.W : 474.39
SMILES Code : BrC1=CC(N2C3=C(C4=C2C=CC(C5=CC=CC=C5)=C4)C=C(C6=CC=CC=C6)C=C3)=CC=C1

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Application In Synthesis of [ 928050-07-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 928050-07-1 ]

[ 928050-07-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56525-79-2 ]
  • [ 591-18-4 ]
  • [ 928050-07-1 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In hexane; dichloromethane; Example 9 Synthesis of Carbazole Derivative 9 3,6-Diphenylcarbazole (2.80 g, 8.77 mmol), 1-bromo-3-iodobenzene (22.18 g, 87.7 mmol), copper powder (0.279 g) and potassium carbonate (4.85 g) were mixed together, and the mixture was heated in a nitrogen atmosphere at 190° C. for 9 hours. The resultant mixture was cooled to room temperature and diluted with methylene chloride, followed by washing with water and drying, to thereby obtain a pale brown liquid. Next, the obtained liquid is purified through silica gel column chromatography using a solvent mixture of methylene chloride/hexane (2/3 by volume), to thereby obtain 3.59 g of 9-(3-bromophenyl)-<strong>[56525-79-2]3,6-diphenylcarbazole</strong>.
3.59 g With copper; potassium carbonate; at 190℃; for 9h;Inert atmosphere; 3,6-Diphenylcarbazole (2.80 g, 8.77 mmol), 1-bromo-3-iodobenzene (22.18 g, 87.7 mmol), copper powder (0.279 g) and potassium carbonate (4.85 g) were mixed together, and the mixture was heated in a nitrogen atmosphere at 190° C. for 9 hours. The resultant mixture was cooled to room temperature and diluted with methylene chloride, followed by washing with water and drying, to thereby obtain a pale brown liquid. Next, the obtained liquid is purified through silica gel column chromatography using a solvent mixture of methylene chloride/hexane (2/3 by volume), to thereby obtain 3.59 g of 9-(3-bromophenyl)-<strong>[56525-79-2]3,6-diphenylcarbazole</strong>.
 

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