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Chemical Structure| 1353658-81-7 Chemical Structure| 1353658-81-7
Chemical Structure| 1353658-81-7

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Product Details of PCy3 Pd G2

CAS No. :1353658-81-7
Formula : C30H43ClNPPd
M.W : 590.52
SMILES Code : C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C1=CC=C([C-]=C1)C2=CC=CC=C2N.Cl[Pd+]
MDL No. :MFCD21363051

Safety of PCy3 Pd G2

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of PCy3 Pd G2

* 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 [ 1353658-81-7 ]

[ 1353658-81-7 ] Synthesis Path-Downstream   1~1

  • 1
  • sodium tetrachloropalladate(II) [ No CAS ]
  • tricyclohexylchlorophosphane [ No CAS ]
  • [ 90-41-5 ]
  • [ 1353658-81-7 ]
YieldReaction ConditionsOperation in experiment
98.8% 1. Add 17.49g (0.103mol) of 2-aminobiphenyl and sodium chloropalladate containing 10g of metal palladium (0.094mol) to 300g (316mL) of N, N-dimethylformamide, and heat to The reaction was stirred at 80 C. for 60 min, and then the reaction system was cooled to normal temperature and suction filtered to dryness.2. Disperse the filter cake obtained in step 1 into 316mL of acetone, add 13.94g (0.329mol) of lithium chloride, stir the reaction at 20 C for 3h under the protection of nitrogen, and then add 32.55g (0.103mol) of tricyclohexylphosphonium chloride Under nitrogen protection, the reaction was stirred for 6 h at 20 C. After the reaction, the solution was filtered, and the filtrate was concentrated to dryness, and then dried at 50 C for 8 hours under a vacuum of 0.08 MPa to obtain an off-white powdery product of chlorine [(tricyclohexylphosphine) -2- (2-aminobiphenyl)] palladium. (II), the yield is 98.8%, the purity is 99.2%,
 

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