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HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4]

Base Information
  • Chemical Name:HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4]
  • CAS No.:869383-17-5
  • Molecular Formula:C45H53N3
  • Molecular Weight:635.936
  • Hs Code.:
HN<sub>3</sub>(2,6-Mes<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)[2-(2,4,6-iPr<sub>3</sub>C<sub>6</sub>H<sub>2</sub>)C<sub>6</sub>H<sub>4</sub>]

Synonyms:HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4]

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Chemical Property of HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4]
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Technology Process of HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4]

There total 1 articles about HN3(2,6-Mes2C6H3)[2-(2,4,6-iPr3C6H2)C6H4] 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:
2'-iodo-2,4,6-triisopropyl-1,1'-biphenyl; With n-butyllithium; In diethyl ether; hexane; at 0 ℃; for 2h;
2'-azido-2,4,6,2'',4'',6''-hexamethyl-[1,1';3',1'']terphenyl; In diethyl ether; hexane; at 0 - 20 ℃;
DOI:10.1002/anie.200501494
Guidance literature:
With nBuLi; In diethyl ether; hexane; byproducts: LiI, nBuH; under Ar, using Schlenk technique; to stirred cooled soln. of triazene deriv. in ethyl ether added n-BuLi in hexane; stirred for 30 min; HgCl2 added, stirred at ambient temp. for 4 h; volatile materials removed under reduced pressure; solid extd. with n-heptane; LiI separated by centrifugation, filtrate concd., cooled at -20°C;
DOI:10.1002/zaac.200900482
Guidance literature:
With nBuLi; In diethyl ether; hexane; byproducts: LiCl, nBuH; under Ar, using Schlenk technique; to stirred cooled soln. of triazene deriv. in ethyl ether added n-BuLi in hexane; stirred for 30 min; HgCl2 added, stirred at ambient temp. for 4 h; volatile materials removed under reduced pressure; solid extd. with n-heptane; LiCl separated by centrifugation, filtrate concd., cooled at -20°C;
DOI:10.1002/zaac.200900482
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