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4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine

Base Information
  • Chemical Name:4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine
  • CAS No.:254450-32-3
  • Molecular Formula:C24H20N2O2
  • Molecular Weight:368.435
  • Hs Code.:
4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine

Synonyms:4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine

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Chemical Property of 4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine
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Technology Process of 4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine

There total 5 articles about 4,4'-bis(p-methoxyphenyl)-2,2'-bipyridine 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:
4,4'-dibromo-2,2'-bipyridine; 4-methoxyphenylboronic acid; With sodium carbonate; In water; toluene; for 0.25h; Inert atmosphere;
With tetrakis(triphenylphosphine) palladium(0); In water; toluene; for 14h; Reflux;
DOI:10.1021/ic101909e
Guidance literature:
Multi-step reaction with 2 steps
1.1: phosphorus tribromide / acetonitrile / 4 h / Reflux
2.1: sodium carbonate / water; toluene / 0.25 h / Inert atmosphere
2.2: 14 h / Reflux
With phosphorus tribromide; sodium carbonate; In water; toluene; acetonitrile; 2.2: Suzuki coupling;
DOI:10.1021/ic101909e
Guidance literature:
Multi-step reaction with 5 steps
1.1: dihydrogen peroxide / acetic acid
2.1: sulfuric acid; nitric acid
3.1: Acetyl bromide / acetic acid / 4 h / 100 °C
4.1: phosphorus tribromide / acetonitrile / 4 h / Reflux
5.1: sodium carbonate / water; toluene / 0.25 h / Inert atmosphere
5.2: 14 h / Reflux
With Acetyl bromide; sulfuric acid; dihydrogen peroxide; nitric acid; phosphorus tribromide; sodium carbonate; In water; acetic acid; toluene; acetonitrile; 5.2: Suzuki coupling;
DOI:10.1021/ic101909e
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