Technology Process of 2,7-dibutyl-1,6-bis(4-methoxyphenyl)naphtho[1,2-b:5,6-b']dithiophene
There total 5 articles about 2,7-dibutyl-1,6-bis(4-methoxyphenyl)naphtho[1,2-b:5,6-b']dithiophene which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
(1,3-diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(ll) dichloride; potassium carbonate;
In
toluene;
at 100 ℃;
for 40h;
Inert atmosphere;
DOI:10.1021/jo400205j
- Guidance literature:
-
Multi-step reaction with 4 steps
1: trans-bis(triphenylphosphine)palladium dichloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide; tetrahydrofuran / 19 h / 100 °C
2: dichloromethane / 13 h / -10 - 20 °C / Inert atmosphere
3: trifluorormethanesulfonic acid / 1,2-dichloro-ethane / 17 h / 60 °C
4: (1,3-diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(ll) dichloride; potassium carbonate / toluene / 40 h / 100 °C / Inert atmosphere
With
copper(l) iodide; trans-bis(triphenylphosphine)palladium dichloride; trifluorormethanesulfonic acid; (1,3-diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;
1: |Sonogashira Cross-Coupling / 4: |Suzuki-Miyaura Coupling;
DOI:10.1021/jo400205j
- Guidance literature:
-
Multi-step reaction with 3 steps
1: dichloromethane / 13 h / -10 - 20 °C / Inert atmosphere
2: trifluorormethanesulfonic acid / 1,2-dichloro-ethane / 17 h / 60 °C
3: (1,3-diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(ll) dichloride; potassium carbonate / toluene / 40 h / 100 °C / Inert atmosphere
With
trifluorormethanesulfonic acid; (1,3-diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(ll) dichloride; potassium carbonate;
In
dichloromethane; 1,2-dichloro-ethane; toluene;
3: |Suzuki-Miyaura Coupling;
DOI:10.1021/jo400205j