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(5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene

Base Information Edit
  • Chemical Name:(5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene
  • CAS No.:936619-45-3
  • Molecular Formula:C20H30O3
  • Molecular Weight:318.456
  • Hs Code.:
  • Mol file:936619-45-3.mol
(5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene

Synonyms:(5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene

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Chemical Property of (5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene Edit
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Technology Process of (5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene

There total 9 articles about (5E,2'Z)-1-methoxy-4-[6-(4-methyl-pent-2-enyloxy)-hex-5-enyloxymethyl]-benzene 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: 89 percent / potassium hydroxide / dimethylsulfoxide / 16 h / 0 - 20 °C
2: 96 percent / oxalyl chloride; dimethyl sulfoxide; triethylamine / CH2Cl2 / -78 - 0 °C
3: 72 percent / chromium(III) chloride; superhydride / tetrahydrofuran / 3 h / 0 °C
4: 81 percent / copper(I) iodide; 3,4,7,8-tetramethyl-1,10-phenanthroline; cesium carbonate / o-xylene / 60 h / 90 °C
With potassium hydroxide; copper(l) iodide; oxalyl dichloride; 3,4,7,8-Tetramethyl-o-phenanthrolin; chromium(III) chloride; lithium triethylborohydride; caesium carbonate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; o-xylene; dimethyl sulfoxide; 4: Buchwald coupling;
DOI:10.1021/ol0702977
Guidance literature:
Multi-step reaction with 3 steps
1: diethyl ether
2: 13.2 g / di-isobutylaluminium hydride / CH2Cl2; diethyl ether / 1 h / -78 °C
3: 81 percent / copper(I) iodide; 3,4,7,8-tetramethyl-1,10-phenanthroline; cesium carbonate / o-xylene / 60 h / 90 °C
With copper(l) iodide; diisobutylaluminum hydride; 3,4,7,8-Tetramethyl-o-phenanthrolin; caesium carbonate; In diethyl ether; dichloromethane; o-xylene; 3: Buchwald coupling;
DOI:10.1021/ol0702977
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