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[4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)]

Base Information Edit
  • Chemical Name:[4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)]
  • CAS No.:919774-03-1
  • Molecular Formula:C41H44NiO2P2S2Si
  • Molecular Weight:781.654
  • Hs Code.:
  • Mol file:919774-03-1.mol
[4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)]

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Chemical Property of [4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)] Edit
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Technology Process of [4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)]

There total 1 articles about [4'-(tert-butyldimethylsilyloxy)-acetophenono-1,1'-ethenedithiolato-Ni(1,2-bis(diphenylphosphino)-ethane)] 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 KO(t)Bu; In diethyl ether; dichloromethane; all manipulations under Ar atm.; KO(t)Bu in Et2O dropped to mixt. of org. compd. and CS2 in Et2O at -70°C, stirred for 1 h then for 1 h at room temp., suspn. of Ni compd. in CH2Cl2 added to suspn. of org. compd., stirred at room temp. for 4 h; water added to suspn. (dissolved), org. phase washed with H2O, org. phase dried with Na2SO4 then solvents evapd., oily residue crystd. by small amt. of CH2Cl2 and excess of pentane; elem. anal.;
DOI:10.1002/zaac.200500509
Guidance literature:
With TBAF; aq. H2SO4; In tetrahydrofuran; all manipulations under Ar atm.; 2 equiv. Bu4NF added to soln. of metal compd., stirred at room temp. for 5 d then aq. H2SO4 added and stirred for 3 h; soln. extd. with CH2Cl2, org. phase washed with water, dried over Na2SO4, solvent evapd., recrystd. from CH2Cl2/pentane; elem. anal.;
DOI:10.1002/zaac.200500509
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