Technology Process of C49H62O10Si
There total 7 articles about C49H62O10Si 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
benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide;
In
acetonitrile;
at 20 ℃;
for 24h;
Inert atmosphere;
DOI:10.1039/c1ob06047c
- Guidance literature:
-
Multi-step reaction with 2 steps
1: toluene / 16 h / Reflux
2: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide / acetonitrile / 24 h / 20 °C / Inert atmosphere
With
benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide;
In
toluene; acetonitrile;
DOI:10.1039/c1ob06047c
- Guidance literature:
-
Multi-step reaction with 5 steps
1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / tetrahydrofuran / 20 h / 20 °C / Inert atmosphere
2: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / N,N-dimethyl-formamide / 48 h / 70 °C / Inert atmosphere
3: potassium carbonate / methanol; dichloromethane / 3.5 h
4: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / diethyl ether / 16 h / 20 °C / Inert atmosphere
5: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide / acetonitrile / 24 h / 20 °C / Inert atmosphere
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); potassium carbonate; benzotriazol-1-ol; triethylamine; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
1: Sonogashira coupling / 2: Sonogashira coupling / 4: Sonogashira coupling;
DOI:10.1039/c1ob06047c