Technology Process of 3-n-Undecylthiophene
There total 2 articles about 3-n-Undecylthiophene which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
pyridine N-oxide; [2,2]bipyridinyl; potassium fluoride; lithium chloride; nickel dichloride; zinc;
In
N,N-dimethyl acetamide;
at 0 - 25 ℃;
for 24h;
DOI:10.1021/acscatal.8b03396
- Guidance literature:
-
With
1,3-bis[(diphenylphosphino)propane]dichloronickel(II);
In
tetrahydrofuran;
for 15h;
Reflux;
DOI:10.1039/c3sc50664a
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: N-Bromosuccinimide / tetrahydrofuran / 15 h / 25 °C
2.1: magnesium / tetrahydrofuran / 0.5 h / Reflux
2.2: 15 h / Reflux
3.1: boron tribromide / dichloromethane / 24 h / -78 - 25 °C
4.1: potassium carbonate / acetonitrile / 6 h / Reflux
5.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / water; acetone / 25 °C
6.1: pyridinium p-toluenesulfonate; toluene-4-sulfonic acid / 24 h / 25 °C
7.1: n-butyllithium; copper dichloride / tetrahydrofuran / 15 h / -60 °C / Reflux
8.1: hydrogenchloride / water; methanol / 24 h / 25 °C
With
hydrogenchloride; N-Bromosuccinimide; osmium(VIII) oxide; n-butyllithium; pyridinium p-toluenesulfonate; boron tribromide; potassium carbonate; toluene-4-sulfonic acid; magnesium; 4-methylmorpholine N-oxide; copper dichloride;
In
tetrahydrofuran; methanol; dichloromethane; water; acetone; acetonitrile;
2.2: |Kumada Cross-Coupling;
DOI:10.1039/c3sc50664a