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Chemical Structure| 1158227-56-5 Chemical Structure| 1158227-56-5

Structure of 1158227-56-5

Chemical Structure| 1158227-56-5

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Product Details of [ 1158227-56-5 ]

CAS No. :1158227-56-5
Formula : C24H15Br
M.W : 383.28
SMILES Code : BrC1=CC=C(C2=CC=C3C4=CC=CC=C4C5=CC=CC=C5C3=C2)C=C1
MDL No. :MFCD28975105
InChI Key :FWESVNIHRVSDDV-UHFFFAOYSA-N
Pubchem ID :58174854

Safety of [ 1158227-56-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 1158227-56-5 ]

* 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 [ 1158227-56-5 ]

[ 1158227-56-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 106-37-6 ]
  • [ 654664-63-8 ]
  • [ 1158227-56-5 ]
YieldReaction ConditionsOperation in experiment
89% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In 1,4-dioxane; water; for 12h;Inert atmosphere; Reflux; In 500 ml three-necked flask, 1,4-dibromobenzene 34.7g (0.147mol), triphenylene-2-yl boronicacid 20.0 g (73.5mmol) and tetrakis(triphenylphosphine) palladium 1.7g (0.08mmol) were charged, potassium carbonate (K2CO3) 15.2g (0.110mmol) and 250 mLof 1,4-dioxane was added under nitrogen gas stream, and the mixture was stirred under reflux for 12 hours with 25mL purified water. After completion of the reaction, the reaction solution was slowly cooled to room temperature and filtered. The filtered solids were washed with methanol and purified water, and recrystallized with dichloromethane and methanol to obtain intermediate compound [1-1] 25.0 g (89%) as white solid.
77% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; at 65℃; for 18h; 1,4-Dibromobenzene (2.4 g, 0.010 mol) in triphenylen-2-ylboronic acid (3.3 g, 0.012mol), Pd (pph3) 4 (0.6 g, 0.0005 mol), potassium carbonate (2.8 g, 0.020 mol) in THFadd 100 mL was reacted with stirring for 18 hours at 65 C. After the reaction cooledto H20: After layer separation the MC column purification (n-Hexane: MC) to yield theintermediate 1-1 2.9 g (yield 77%)
70% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; at 65℃; for 18h; 1,4-dibromobenzene (2.4g, 0.010mol) into the triphenylen-2-ylboronic acid (3.3g, 0.012mol) in synthesis by the same method used in Preparation Example 1-7 to Intermediate 25-2> to give the 2.7g (70% yield).
70% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; at 65℃; for 18h; 1,4-dibromobenzene (2.4 g, 0.010 mol) and Pd (PPh3) 4 (0.6 g, 0.012 mol) were added to triphenylen-2-ylboronic acidG, 0.0005 mol) and potassium carbonate (2.8 g, 0.020 mol) in THF (100 mL), and the mixture was reacted at 65 DEG C for 18 hours with stirring. After completion of the reaction, the reaction mixture was cooled, separated into H 2 O: MC and subjected to column purification (N-HEXANE: MC) to obtain 2.7 g (yield 70%) of Intermediate 1-3.
69% With bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate; In toluene; at 95℃; for 4h; 3-bromo-1H-indole (2.0 g, 0.010 mol) in bromobenzene (1.6 g, 0.010 mol), Pd (dba) 2 (0.5 g, 0.0005 mol), sodium-tert-butoxide (1.9 g, 0.020 mol) in TOL into a 70 mL was reacted with stirring for 4 hours at 95 . After the end of the reaction H20: After layer separation the MC column purification (n-HEXANE: MC) to yield the intermediate 1-1 2.1 g (79%). 1,4-dibromobenzene (1.9 g, 0.008 mol) in triphenylen-2-ylboronic acid (2.7 g, 0.010 mol) into the Example 1-Preparation Example 4 in the same manner used in the synthesis <intermediate 6-1> 2.1 g (yield 69%) of the target compound.

 

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