Technology Process of 5,10,10-triphenyl-5,10-dihydrophenazasiline
There total 4 articles about 5,10,10-triphenyl-5,10-dihydrophenazasiline 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
tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide;
In
benzene;
at 90 ℃;
for 24h;
DOI:10.1071/CH15652
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: copper(l) iodide; potassium carbonate / 5,5-dimethyl-1,3-cyclohexadiene / 48 h / 120 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 1.5 h / -78 °C
2.2: 12.5 h / -78 - 20 °C
3.1: tetra-(n-butyl)ammonium iodide; tert.-butylhydroperoxide / benzene / 24 h / 90 °C
With
tert.-butylhydroperoxide; copper(l) iodide; n-butyllithium; tetra-(n-butyl)ammonium iodide; potassium carbonate;
In
tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; hexane; benzene;
DOI:10.1071/CH15652
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: copper(l) iodide; potassium carbonate / 5,5-dimethyl-1,3-cyclohexadiene / 48 h / 120 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 1.5 h / -78 °C
2.2: 12.5 h / -78 - 20 °C
3.1: tetra-(n-butyl)ammonium iodide; tert.-butylhydroperoxide / benzene / 24 h / 90 °C
With
tert.-butylhydroperoxide; copper(l) iodide; n-butyllithium; tetra-(n-butyl)ammonium iodide; potassium carbonate;
In
tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; hexane; benzene;
DOI:10.1071/CH15652
