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((C6H5)2PCH2)3BC6H5(1-)*(C4H9)4N(1+)=[(C4H9)4N][((C6H5)2PCH2)3BC6H5]

Base Information
  • Chemical Name:((C6H5)2PCH2)3BC6H5(1-)*(C4H9)4N(1+)=[(C4H9)4N][((C6H5)2PCH2)3BC6H5]
  • CAS No.:694484-07-6
  • Molecular Formula:C16H36N*C45H41BP3
  • Molecular Weight:928.021
  • Hs Code.:
((C<sub>6</sub>H<sub>5</sub>)2PCH<sub>2</sub>)3BC<sub>6</sub>H<sub>5</sub><sup>(1-)</sup>*(C<sub>4</sub>H<sub>9</sub>)4N<sup>(1+)</sup>=[(C<sub>4</sub>H<sub>9</sub>)4N][((C<sub>6</sub>H<sub>5</sub>)2PCH<sub>2</sub>)3BC<sub>6</sub>H<sub>5</sub>]

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Chemical Property of ((C6H5)2PCH2)3BC6H5(1-)*(C4H9)4N(1+)=[(C4H9)4N][((C6H5)2PCH2)3BC6H5]
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Technology Process of ((C6H5)2PCH2)3BC6H5(1-)*(C4H9)4N(1+)=[(C4H9)4N][((C6H5)2PCH2)3BC6H5]

There total 1 articles about ((C6H5)2PCH2)3BC6H5(1-)*(C4H9)4N(1+)=[(C4H9)4N][((C6H5)2PCH2)3BC6H5] 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:
With air; In methanol; water; Li-compd. was dissolved in MeOH in air, soln. was filtered via diatomaceous earth, Bu4NBr was added in H2O; solid was taken with addn. of Et2O, stirring (5 min), filtration, washing twice sequentially with H2O, Et2O, solid was dissolved iN MeCN, dried with Na2SO4 (stirring for 10 min with it), soln. was filtered, triturated with Et2O, elem. anal.;
DOI:10.1016/j.poly.2003.11.036
Guidance literature:
In tetrahydrofuran; under N2, 1 equiv. of Pt-compd. in THF was added to THF soln. of B-compd., stirring for 4 h at room temp.; volatiles were removed, pptn. with pentane, solid was triturated with pentane, drying in vac., elem. anal.;
DOI:10.1016/j.poly.2003.11.036
Guidance literature:
In tetrahydrofuran; byproducts: Bu4NI; under N2, Pt- and B-compds. were dissolved in THF, stirring for 2 h; soln. was concd., solid was pptd. upon standing, dried in vac., benzene was added, stirring for 10 min, soln. was filtered, volatiles were removed in vac., elem. anal.;
DOI:10.1016/j.poly.2003.11.036
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