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3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran

Base Information
  • Chemical Name:3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran
  • CAS No.:1427216-08-7
  • Molecular Formula:C17H13IO5
  • Molecular Weight:424.192
  • Hs Code.:
3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran

Synonyms:3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran

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Chemical Property of 3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran
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Technology Process of 3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran

There total 7 articles about 3-((2-iodo-5-methoxyphenoxy)methyl)-5,6-methylene-dioxybenzofuran 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 diisopropyl (E)-azodicarboxylate; triphenylphosphine; In tetrahydrofuran; for 2h; Reflux;
DOI:10.1080/00397911.2012.661910
Guidance literature:
With boron trichloride; In dichloromethane; at -78 ℃; for 0.5h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c6ob01451h
Guidance literature:
Multi-step reaction with 4 steps
1: magnesium chloride; triethylamine / acetonitrile / 6 h / Reflux; Inert atmosphere
2: tetrafluoroboric acid diethyl ether / dichloromethane / 1 h / 25 - 30 °C / Inert atmosphere
3: diisobutylaluminium hydride / dichloromethane; hexane / -78 - 20 °C
4: triphenylphosphine; diisopropyl (E)-azodicarboxylate / tetrahydrofuran / 2 h / Reflux
With tetrafluoroboric acid diethyl ether; diisobutylaluminium hydride; diisopropyl (E)-azodicarboxylate; triethylamine; triphenylphosphine; magnesium chloride; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1080/00397911.2012.661910
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