Technology Process of C14H9NO3
There total 5 articles about C14H9NO3 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
dichloro bis(acetonitrile) palladium(II);
In
acetonitrile;
at 86 ℃;
Inert atmosphere;
DOI:10.1016/j.ejmech.2014.03.059
- Guidance literature:
-
Multi-step reaction with 3 steps
1: potassium carbonate / methanol; dichloromethane
2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 20 °C / Inert atmosphere
3: dichloro bis(acetonitrile) palladium(II) / acetonitrile / 86 °C / Inert atmosphere
With
bis-triphenylphosphine-palladium(II) chloride; dichloro bis(acetonitrile) palladium(II); copper(l) iodide; potassium carbonate; triethylamine;
In
methanol; dichloromethane; acetonitrile;
2: |Sonogashira Cross-Coupling;
DOI:10.1016/j.ejmech.2014.03.059
- Guidance literature:
-
Multi-step reaction with 2 steps
1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 20 °C / Inert atmosphere
2: dichloro bis(acetonitrile) palladium(II) / acetonitrile / 86 °C / Inert atmosphere
With
bis-triphenylphosphine-palladium(II) chloride; dichloro bis(acetonitrile) palladium(II); copper(l) iodide; triethylamine;
In
acetonitrile;
1: |Sonogashira Cross-Coupling;
DOI:10.1016/j.ejmech.2014.03.059