Technology Process of 1-bromo-4-(5-perfluorophenylthien-2-yl)-2,5-dioctyloxybenzene
There total 5 articles about 1-bromo-4-(5-perfluorophenylthien-2-yl)-2,5-dioctyloxybenzene which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran; N,N-dimethyl-formamide / 24 h / 80 °C / Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
2.2: 20 °C
3.1: cesium fluoride; tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / tetrahydrofuran / 72 h / 80 °C / Inert atmosphere
With
tris-(dibenzylideneacetone)dipalladium(0); tetrakis(triphenylphosphine) palladium(0); n-butyllithium; triphenylphosphine; cesium fluoride;
In
tetrahydrofuran; N,N-dimethyl-formamide;
1.1: |Stille Cross Coupling;
DOI:10.1002/chem.201203869
- Guidance literature:
-
Multi-step reaction with 2 steps
1: trifluoroacetic acid; N-iodo-succinimide / acetonitrile / 48 h / Reflux
2: cesium fluoride; tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / tetrahydrofuran / 72 h / 80 °C / Inert atmosphere
With
tris-(dibenzylideneacetone)dipalladium(0); N-iodo-succinimide; triphenylphosphine; cesium fluoride; trifluoroacetic acid;
In
tetrahydrofuran; acetonitrile;
DOI:10.1002/chem.201203869
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: potassium carbonate / acetonitrile / 1 h / 20 °C
1.2: 18 h / Reflux
2.1: trifluoroacetic acid; N-iodo-succinimide / acetonitrile / 48 h / Reflux
3.1: cesium fluoride; tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine / tetrahydrofuran / 72 h / 80 °C / Inert atmosphere
With
tris-(dibenzylideneacetone)dipalladium(0); N-iodo-succinimide; potassium carbonate; triphenylphosphine; cesium fluoride; trifluoroacetic acid;
In
tetrahydrofuran; acetonitrile;
DOI:10.1002/chem.201203869