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4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane

Base Information
  • Chemical Name:4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane
  • CAS No.:124243-39-6
  • Molecular Formula:C33H43N3O2
  • Molecular Weight:513.723
  • Hs Code.:
4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane

Synonyms:4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane

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Chemical Property of 4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane
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Technology Process of 4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane

There total 5 articles about 4,10,14-tribenzyl-12-methylene-4,10,14-triaza-1,7-dioxacyclohexadecane 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 3 steps
1: 55 percent / sodium carbonate, sodium iodide / acetonitrile / 48 h / Heating
2: lithium aluminum hydride / tetrahydrofuran / 24 h / Heating
3: 63 percent / sodium carbonate , sodium iodide / acetonitrile / 24 h / Heating
With lithium aluminium tetrahydride; sodium carbonate; sodium iodide; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jo00278a016
Guidance literature:
Multi-step reaction with 4 steps
1: 65 percent / SOCl2 / CHCl3 / 1.) room temp., 1 h, 2.) reflux, 4 h
2: 55 percent / sodium carbonate, sodium iodide / acetonitrile / 48 h / Heating
3: lithium aluminum hydride / tetrahydrofuran / 24 h / Heating
4: 63 percent / sodium carbonate , sodium iodide / acetonitrile / 24 h / Heating
With lithium aluminium tetrahydride; thionyl chloride; sodium carbonate; sodium iodide; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1021/jo00278a016
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