Technology Process of C24H15NO
There total 5 articles about C24H15NO 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
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine;
In
toluene;
at 55 ℃;
Inert atmosphere;
DOI:10.1246/cl.140579
- Guidance literature:
-
Multi-step reaction with 3 steps
1: tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine; copper(l) iodide / toluene / 55 °C / Inert atmosphere
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 4 h / 0 - 20 °C / Inert atmosphere
3: tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine; copper(l) iodide / toluene / 55 °C / Inert atmosphere
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; toluene;
1: |Sonogashira Cross-Coupling / 3: |Sonogashira Cross-Coupling;
DOI:10.1246/cl.140579
- Guidance literature:
-
Multi-step reaction with 4 steps
1: methylmagnesium bromide / tetrahydrofuran; diethyl ether / 0.5 h / 0 °C / Inert atmosphere
2: tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine; copper(l) iodide / toluene / 55 °C / Inert atmosphere
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 4 h / 0 - 20 °C / Inert atmosphere
4: tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine; copper(l) iodide / toluene / 55 °C / Inert atmosphere
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); methylmagnesium bromide; tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; diethyl ether; toluene;
2: |Sonogashira Cross-Coupling / 4: |Sonogashira Cross-Coupling;
DOI:10.1246/cl.140579