Technology Process of C31H48O4Si
There total 12 articles about C31H48O4Si which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
Et3CONa;
In
5,5-dimethyl-1,3-cyclohexadiene;
Reflux;
DOI:10.1021/ol103151k
- Guidance literature:
-
Multi-step reaction with 7 steps
1: toluene / 1 h / Reflux
2: 10% Pd(OH)2 on carbon; hydrogen / ethanol / 6 h / 20 °C
3: caesium carbonate / dimethyl sulfoxide / 3 h / 20 - 50 °C
4: 2,6-dimethylpyridine; lithium iodide / 10.5 h / Reflux
5: ammonium fluoride / methanol / 13.5 h / 20 °C
6: tetrachloromethane; triphenylphosphine / 19 h / Reflux
7: Et3CONa / 5,5-dimethyl-1,3-cyclohexadiene / Reflux
With
2,6-dimethylpyridine; tetrachloromethane; ammonium fluoride; 10% Pd(OH)2 on carbon; hydrogen; caesium carbonate; triphenylphosphine; Et3CONa; lithium iodide;
In
methanol; 5,5-dimethyl-1,3-cyclohexadiene; ethanol; dimethyl sulfoxide; toluene;
DOI:10.1021/ol103151k
- Guidance literature:
-
Multi-step reaction with 7 steps
1: diisobutylaluminium hydride / toluene / 4 h / -78 °C
2: 1H-imidazole / N,N-dimethyl-formamide / 1 h / 20 °C
3: caesium carbonate / dimethyl sulfoxide / 3 h / 20 - 50 °C
4: 2,6-dimethylpyridine; lithium iodide / 10.5 h / Reflux
5: ammonium fluoride / methanol / 13.5 h / 20 °C
6: tetrachloromethane; triphenylphosphine / 19 h / Reflux
7: Et3CONa / 5,5-dimethyl-1,3-cyclohexadiene / Reflux
With
1H-imidazole; 2,6-dimethylpyridine; tetrachloromethane; ammonium fluoride; diisobutylaluminium hydride; caesium carbonate; triphenylphosphine; Et3CONa; lithium iodide;
In
methanol; 5,5-dimethyl-1,3-cyclohexadiene; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ol103151k