Technology Process of diethyl 2,2′-5′,2′′-terthiophene-4,4′′-bis(p-tbutylphenyl)-5,5′′-dicarboxylate
There total 3 articles about diethyl 2,2′-5′,2′′-terthiophene-4,4′′-bis(p-tbutylphenyl)-5,5′′-dicarboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
1,8-diazabicyclo[5.4.0]undec-7-ene;
In
ethanol;
at 70 ℃;
for 20h;
Inert atmosphere;
Schlenk technique;
DOI:10.1039/c3ob40124c
- Guidance literature:
-
Multi-step reaction with 2 steps
1: tetrakis(triphenylphosphine) palladium(0); copper(l) iodide; triethylamine / tetrahydrofuran / 4.25 h / 20 °C / Inert atmosphere; Schlenk technique
2: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 20 h / 70 °C / Inert atmosphere; Schlenk technique
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine;
In
tetrahydrofuran; ethanol;
1: |Sonogashira Cross-Coupling / 2: |Fiesselmann Thiophene Synthesis;
DOI:10.1039/c3ob40124c
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: potassium hydroxide / water; methanol / 0.5 h / 20 °C / Inert atmosphere; Schlenk technique
1.2: Inert atmosphere; Sealed tube
2.1: tetrakis(triphenylphosphine) palladium(0); copper(l) iodide; triethylamine / tetrahydrofuran / 4.25 h / 20 °C / Inert atmosphere; Schlenk technique
3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 20 h / 70 °C / Inert atmosphere; Schlenk technique
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; potassium hydroxide;
In
tetrahydrofuran; methanol; ethanol; water;
2.1: |Sonogashira Cross-Coupling / 3.1: |Fiesselmann Thiophene Synthesis;
DOI:10.1039/c3ob40124c