Technology Process of C31H39IO3Si
There total 11 articles about C31H39IO3Si 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:
-
Multi-step reaction with 8 steps
2: toluene-4-sulfonic acid
3: copper(l) iodide; potassium carbonate; sodium iodide / N,N-dimethyl-formamide / 20 °C
4: methanol / dichloromethane / 20 °C
5: quinoline; hydrogen / ethyl acetate / 20 °C
6: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C
7: toluene / 2 h / Reflux
8: chromium dichloride / tetrahydrofuran / 0 °C
With
quinoline; chromium dichloride; methanol; copper(l) iodide; oxalyl dichloride; hydrogen; potassium carbonate; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; sodium iodide;
In
tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;
1: Jones oxidation / 5: Lindlar hydrogenation / 6: Swern oxidation / 7: Wittig homologation / 8: Takai olefination;
DOI:10.1016/j.tetlet.2012.01.032
- Guidance literature:
-
Multi-step reaction with 7 steps
1: toluene-4-sulfonic acid
2: copper(l) iodide; potassium carbonate; sodium iodide / N,N-dimethyl-formamide / 20 °C
3: methanol / dichloromethane / 20 °C
4: quinoline; hydrogen / ethyl acetate / 20 °C
5: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C
6: toluene / 2 h / Reflux
7: chromium dichloride / tetrahydrofuran / 0 °C
With
quinoline; chromium dichloride; methanol; copper(l) iodide; oxalyl dichloride; hydrogen; potassium carbonate; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; sodium iodide;
In
tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;
4: Lindlar hydrogenation / 5: Swern oxidation / 6: Wittig homologation / 7: Takai olefination;
DOI:10.1016/j.tetlet.2012.01.032