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2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene

Base Information Edit
  • Chemical Name:2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene
  • CAS No.:1333332-91-4
  • Molecular Formula:C30H42O2S2
  • Molecular Weight:498.794
  • Hs Code.:
  • Mol file:1333332-91-4.mol
2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene

Synonyms:2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene

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Chemical Property of 2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene Edit
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Technology Process of 2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene

There total 6 articles about 2,2'-(4,5-dioctyloxy-1,2-phenylene)dithiophene 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:
thiophene; With n-butyllithium; In 1,2-dimethoxyethane; hexane; at 0 - 20 ℃;
With zinc(II) chloride; In 1,2-dimethoxyethane; hexane; at 20 ℃; for 1h; Inert atmosphere;
1,2-Dibromo-4,5-bis(octyloxy)benzene; With tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; hexane; for 12h; Reflux;
DOI:10.1021/ol202236r
Guidance literature:
With tetrakis(triphenylphosphine) palladium(0); In toluene; at 120 ℃; for 24h; Inert atmosphere;
DOI:10.1016/j.polymer.2018.06.007
Guidance literature:
Multi-step reaction with 3 steps
1.1: bromine / chloroform
2.1: potassium carbonate / butanone / 0.5 h / 20 °C
2.2: 12 h / Reflux
3.1: n-butyllithium / 1,2-dimethoxyethane; hexane / 0 - 20 °C
3.2: 1 h / 20 °C / Inert atmosphere
3.3: 12 h / Reflux
With n-butyllithium; bromine; potassium carbonate; In 1,2-dimethoxyethane; hexane; chloroform; butanone; 3.1: Negishi coupling reaction / 3.2: Negishi coupling reaction / 3.3: Negishi coupling reaction;
DOI:10.1021/ol202236r
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