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Benzenamine, N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)-

Base Information
  • Chemical Name:Benzenamine, N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)-
  • CAS No.:494191-96-7
  • Molecular Formula:C29H34NP
  • Molecular Weight:427.569
  • Hs Code.:
Benzenamine,
N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)-

Synonyms:

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Chemical Property of Benzenamine, N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)-
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Technology Process of Benzenamine, N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)-

There total 1 articles about Benzenamine, N-[2-(diphenylphosphino)cyclopentylidene]-2,6-bis(1-methylethyl)- 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:
N-(2,6-diisopropylphenyl)cyclopentylideneimine; With lithium diisopropyl amide; In diethyl ether; at -78 ℃; Inert atmosphere;
chloro-diphenylphosphine; In diethyl ether; at -78 ℃; Inert atmosphere;
DOI:10.1021/om400688v
Guidance literature:
In dichloromethane; Sonication; under Ar; 0.4 mmol of Ni-contg. compd. were suspended in CH2Cl2 at room temp. with the aid of an ultrasound bath and slowly reacted with a soln.of 1.00 equiv. of a ligand in the same solvent; stirring for 1 h; the soln. was filtered and the filtrate was concd., washed with n-pentane and dried in vac.; the complex was crystd. from CH2Cl2; elem. anal.;
DOI:10.1016/S0022-328X(02)01903-4
Guidance literature:
In dichloromethane; byproducts: 1,5-cyclooctadiene; under Ar; to a soln. of Pd-contg. compd. (1.990 mmol) in CH2Cl2 kept under stirring, a soln. of a ligand (1.990 mmol) in the same solvent was added dropwise at room temp.; stirring for 30 min; the solvent was reduced in vac.; the complex was pptd. by addn. of n-pentane; the solid was filtered, washed with pentane and dried; elem. anal.;
DOI:10.1016/S0022-328X(02)01903-4
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