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2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6)

Base Information Edit
  • Chemical Name:2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6)
  • CAS No.:770742-90-0
  • Molecular Formula:C24H30B2IP
  • Molecular Weight:498.002
  • Hs Code.:
  • Mol file:770742-90-0.mol
2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane<sup>(6)</sup>

Synonyms:2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6)

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Chemical Property of 2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6) Edit
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Technology Process of 2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6)

There total 1 articles about 2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6) 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 n-BuLi; In hexane; (inert atm.), HPPh2 and n-BuLi mixed in hexane, cooled to -60°C, added to borane in hexane, warmed to room temp., stirred overnight; filtered, dried (vac.), elem. anal.;
DOI:10.1002/ejic.200300938
Guidance literature:
lithium phenylacetylide; With zinc(II) chloride; In tetrahydrofuran; at 20 ℃; for 3h;
2,3,4,5-tetraethyl-1-iodo-6-(diphenylphosphanyl)-2,3,4,5-tetracarba-nido-hexaborane(6); tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; for 240h; Heating;
DOI:10.1002/ejic.200500787
Guidance literature:
With ZnCl2; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; N2, to a soln. of acetylide added at room temp. ZnCl2, stirred for 2 h, a soln. added to a mixt. of B and Pd compds., refluxed for 10 d; solvent removed (high vac.), extd. (hexane), filtered, evapd. to dryness(vac.); NMR;
DOI:10.1002/ejic.200500787
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