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1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide

Base Information
  • Chemical Name:1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide
  • CAS No.:1403575-24-5
  • Molecular Formula:Br*C30H45N4O
  • Molecular Weight:557.618
  • Hs Code.:
1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide

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Chemical Property of 1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide
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Technology Process of 1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide

There total 5 articles about 1-{4-[3-(5-dodecylpyrimidin-2-yl)phenoxy]butyl}-3-methylimidazolium bromide 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:
Multi-step reaction with 4 steps
1.1: trichlorophosphate / 40 °C / Inert atmosphere; Cooling with ice
1.2: 2 h / 40 - 60 °C / Inert atmosphere
2.1: sodium methylate / methanol / 14 h / 20 °C / Inert atmosphere; Reflux
3.1: potassium hydroxide / dimethyl sulfoxide / 0.17 h / 20 °C / Inert atmosphere
3.2: 12 h / 20 °C / Inert atmosphere
4.1: acetonitrile / 72 h / 60 °C / Inert atmosphere
With sodium methylate; potassium hydroxide; trichlorophosphate; In methanol; dimethyl sulfoxide; acetonitrile;
DOI:10.1039/c2jm34595a
Guidance literature:
Multi-step reaction with 2 steps
1.1: potassium hydroxide / dimethyl sulfoxide / 0.17 h / 20 °C / Inert atmosphere
1.2: 12 h / 20 °C / Inert atmosphere
2.1: acetonitrile / 72 h / 60 °C / Inert atmosphere
With potassium hydroxide; In dimethyl sulfoxide; acetonitrile;
DOI:10.1039/c2jm34595a
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