Alternatived Products of [ 1141757-83-6 ]
Product Details of [ 1141757-83-6 ]
CAS No. : | 1141757-83-6 |
MDL No. : | |
Formula : |
C54H35N3
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | FXKMXDQBHDTQII-UHFFFAOYSA-N |
M.W : | 725.88 |
Pubchem ID : | 68185634 |
Synonyms : |
|
Safety of [ 1141757-83-6 ]
Application In Synthesis of [ 1141757-83-6 ]
* 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 [ 1141757-83-6 ]
- 1
-
[ 1153-85-1 ]

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[ 618442-57-2 ]

-
[ 1141757-83-6 ]
Yield | Reaction Conditions | Operation in experiment |
82% |
|
(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) -9-phenylcarbazole,One equivalent (20 g, 40.49 mmol),3-Bromo-9-phenylcarbazole, 2Equivalent (26 g, 81 mmol), 33.5 g of K2CO3, 800 ml of toluene,And 200 ml of water was added to a 2-L 2-neck round bottom flask. The mixture was stirred at room temperature for 30 minutes,Pd (PPh3) 4 (1.4 g, 1.21 mmol) was added and refluxed for 24 hours.After the reaction was completed, the reaction mixture was extracted with methylene chloride, added with MgSO 4 and filtered.After removing the solvent of the obtained organic layer, it was purified by column chromatography to obtain intermediate compound 1 (24.80 g, yield 82%). |
- 2
-
[ 1126522-69-7 ]

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[ 57103-20-5 ]

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[ 1141757-83-6 ]
Yield | Reaction Conditions | Operation in experiment |
60.9% |
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 5h;Reflux; Inert atmosphere; |
Synthesis Example 1 Synthesis of H1-1 compound: 1.6 g of 3,6-dibromo-9-phenyl-9oxazole, 2.4 g of 9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9Eta-carbazole under a nitrogen atmosphere ,0.23 g of tetrakis(triphenylphosphine)palladium, 6 ml of 2M aqueous potassium carbonate solution,20 ml of toluene and 5 ml of ethanol were placed in a reaction vessel, and then heated and stirred at reflux temperature for 5 hours.After cooling to 40 C, the insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to give a crude product.The crude product was purified by recrystallization (solvent: toluene/methanol) and dried.1.76 g (yield: 60.9%) of 3,6-bis(9'-phenyl-9Eta-carbazol-3-yl)-9-phenyl-9H-carbazole (Compound H1-1) is obtained as a brownish white powder. |