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Chemical Structure| 17425-91-1 Chemical Structure| 17425-91-1

Structure of 17425-91-1

Chemical Structure| 17425-91-1

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Product Details of [ 17425-91-1 ]

CAS No. :17425-91-1
Formula : C15H19NSi
M.W : 241.40
SMILES Code : C[Si](C)(C)N(C1=CC=CC=C1)C2=CC=CC=C2

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Application In Synthesis of [ 17425-91-1 ]

* 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 [ 17425-91-1 ]

[ 17425-91-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 104-92-7 ]
  • [ 17425-91-1 ]
  • [ 4316-51-2 ]
YieldReaction ConditionsOperation in experiment
94% With cesium fluoride; bis(dibenzylideneacetone)-palladium(0); XPhos; at 100℃; for 1h;Inert atmosphere; General procedure: A general procedure for the synthesis of arylamines. To a mixture of aryl halide 1 (0.50 mmol), CsF (0.75 mmol), Pd(dba)2 (5.0mumol), Xphos (10 mumol), and DMI (0.50 mL) in a screw vial was added N-trimethylsilylamine 2 (0.55 mmol), and the mixture was stirred at 100 C for the time specified in Tables 1 and 2. The resultant mixture was quenched with H2O. The aqueous layer was extracted with Et2O, and washed with brine. The combined organic layers were dried over anhydrous MgSO4. After concentration in vacuo, the residue was purified by flash chromatography on silica gel or preparative TLC to afford arylamine 3.
67% With bis(1,5-cyclooctadiene)nickel (0); 1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene hydrochloride; potassium tert-butylate; cesium fluoride; at 100℃; for 36h;Inert atmosphere; General procedure: A mixture of Ni(cod)2 (0.050 mmol), SIPr·HCl (0.050 mmol),KOt-Bu (0.050 mmol), and CPME was stirred at 100 C for 30min. To this was added NaOAc (0.85 mmol), aryl bromide 1(0.50 mmol), and N-TMS-carbazole 2 (0.65 mmol). The reactionmixture was quenched with H2O. The aqueous layer wasextracted with Et2O and washed with brine. The combinedorganic layers were dried over anhydrous MgSO4. After concentrationin vacuo, the residue was purified by flash chromatographyon silica gel or preparative TLC to afford N-aryl-carbazoles 3.
 

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