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(E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene

Base Information
  • Chemical Name:(E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene
  • CAS No.:1298086-69-7
  • Molecular Formula:C37H54O12
  • Molecular Weight:690.829
  • Hs Code.:
(E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene

Synonyms:(E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene

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Chemical Property of (E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene
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Technology Process of (E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)benzene

There total 2 articles about (E)-1,2,3-tris[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-5-(4-ethynylstyryl)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:
With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1021/ic102043v
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; oil / 1 h / 50 °C / Inert atmosphere
1.2: 2 h / Inert atmosphere; Reflux
2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; isopropylamine / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere; ultrasound
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrabutyl ammonium fluoride; sodium hydride; isopropylamine; In tetrahydrofuran; oil;
DOI:10.1021/ic102043v
Guidance literature:
With PdCl2(P(C6H5)3)2; CuI; In tetrahydrofuran; triethylamine; Sonication; sonication mixt. of carborane deriv., acetylene deriv., palladium compd.and copper iodide in THF/triethylamine (1:3) for 2 h, stirring for 2 d; evapn., chromy. (alumina, methanol/cyclohexane (1:9)), NMR and MS;
DOI:10.1021/ic102043v
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