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Chemical Structure| 19222-81-2 Chemical Structure| 19222-81-2

Structure of 19222-81-2

Chemical Structure| 19222-81-2

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Product Details of [ 19222-81-2 ]

CAS No. :19222-81-2
Formula : C18H12ClN
M.W : 277.75
SMILES Code : ClC1=CC(N2C3=C(C4=C2C=CC=C4)C=CC=C3)=CC=C1

Safety of [ 19222-81-2 ]

Application In Synthesis of [ 19222-81-2 ]

* 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 [ 19222-81-2 ]

[ 19222-81-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19222-81-2 ]
  • [ 73183-34-3 ]
  • [ 870119-58-7 ]
YieldReaction ConditionsOperation in experiment
75% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 130℃; for 12h;Reflux; 9- (3-chlorophenyl) -9H-carbazole 20 g (72 mmol), 4,4,4 ', 4', 5,5, 5 ', 5'-octamethyl-2,2'-bi (1,3 ,2-dioxaborolane) 20.1 g (79.2 mmol).Pd (dppf) Cl2 2.9 g (3.6 mmol), KOAc 21.2g (216 mmol) was added and 500 mL dioxane was added to the reaction solution. The mixture was heated under reflux for 12 hours at 130C . Then cooled to room temperature and stop the reaction with 300 mL aqueous ammonium chloride solution to the reaction solution. Extract the mixture with E.A 500 mL, and washed with distilled water. The resulting organic layer was dried over anhydrous MgSO4, was evaporated under reduced pressure, and purified by silica gel column chromatography to give the title compound 20.0 g (75% yield).
66% With bis[1,2-bis(diphenylphosphino)ferrocene]-palladium(0); potassium acetate; In N,N-dimethyl-formamide; at 150℃; for 50h;Inert atmosphere; I-6 (145 g, 522 mmol) was dissolved in 1,600 mL of dimethylforamide (DMF) in a nitrogen atmosphere, Bis (pinacolato) diboron (159 g, 626 mmol)And (1,1-bis (diphenylphosphine) ferrocene) dichloropalladium (II) (4.26 g, 5.22 mmol)Potassium acetate (128 g, 1,305 mmol) was added and the mixture was heated at 150 C for 50 hours to reflux. After completion of the reaction, water was added to the reaction solution, the mixture was filtered,And dried in a vacuum oven.The residue thus obtained was separated and purified by flash column chromatography to obtain Compound I-7 (127 g, 66%).
 

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