Technology Process of C29H20ClF5N2O5
There total 10 articles about C29H20ClF5N2O5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
palladium diacetate;
In
toluene;
at 20 - 100 ℃;
for 21h;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: potassium carbonate / 18-crown-6 ether / DMF (N,N-dimethylformamide) / 4 h / 20 °C
2: methanol / 1 h / 20 °C
3: pyridine / dichloromethane
4: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 19 h / 20 - 100 °C
5: hydrogen / palladium 10% on activated carbon / ethanol; ethyl acetate / 0.67 h / 20 °C / 760.05 Torr
6: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 21 h / 20 - 100 °C
With
pyridine; hydrogen; potassium carbonate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
18-crown-6 ether; palladium 10% on activated carbon; palladium diacetate;
In
methanol; DMF (N,N-dimethylformamide); ethanol; dichloromethane; ethyl acetate; toluene;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: potassium carbonate / acetone / 50 h / 20 °C / Reflux
2: potassium carbonate / 18-crown-6 ether / DMF (N,N-dimethylformamide) / 4 h / 20 °C
3: methanol / 1 h / 20 °C
4: pyridine / dichloromethane
5: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 19 h / 20 - 100 °C
6: hydrogen / palladium 10% on activated carbon / ethanol; ethyl acetate / 0.67 h / 20 °C / 760.05 Torr
7: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 21 h / 20 - 100 °C
With
pyridine; hydrogen; potassium carbonate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
18-crown-6 ether; palladium 10% on activated carbon; palladium diacetate;
In
methanol; DMF (N,N-dimethylformamide); ethanol; dichloromethane; ethyl acetate; acetone; toluene;