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N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate

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  • Chemical Name:N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate
  • CAS No.:851539-79-2
  • Molecular Formula:C32H12BF24*C38H30F6N3Pd
  • Molecular Weight:1612.31
  • Hs Code.:
  • Mol file:851539-79-2.mol
N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate

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Chemical Property of N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate Edit
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Technology Process of N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate

There total 1 articles about N,N'-1,2-acenaphthylenediylidene bis(2,6-dimethyl aniline) palladium(II)(methyl)[(3,5-trifluoromethyl phenyl)cyanide] tetra(3,5-trifluoromethyl phenyl)borate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In dichloromethane; byproducts: NaCl; under Ar; CH2Cl2 added to Na borate and Pd complex at -78°C, 3,5-(CF3)2C6H3CN added, allowed to warm to room temp., stirred overnight; soln. filtered, filtrate evapd. under vac., pentane added to oily residue, stirred for 1.5 h, ppt. filtered off and dried under vac. for 3 h; elem. anal.;
DOI:10.1021/om040077m
Guidance literature:
In dichloromethane; (Ar), Pd complex in dry box cooled to 0°C, slowly treated with dry CH2Cl2 and vinyl acetate , stirred for 2 h, warmed to 20°C; chromy.(SiO2 - Et2O), crystd.(CH2Cl2-pentane) at -30°C, elem. anal., NMR; Kinetics;
DOI:10.1021/ja045969s
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