Technology Process of 2,4-bis(p-dodecylphenylamino)-6-chloro-1,3,5-triazine
There total 4 articles about 2,4-bis(p-dodecylphenylamino)-6-chloro-1,3,5-triazine 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
N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 13h;
Inert atmosphere;
DOI:10.1021/ja302574b
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 5%-palladium/activated carbon; hydrogen / ethanol; ethyl acetate / 24 h / 20 °C / 15001.5 Torr / Autoclave
2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 13 h / 0 - 20 °C / Inert atmosphere
With
5%-palladium/activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1021/ja302574b
- Guidance literature:
-
Multi-step reaction with 3 steps
1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / 2 h / 80 °C / Inert atmosphere
2: 5%-palladium/activated carbon; hydrogen / ethanol; ethyl acetate / 24 h / 20 °C / 15001.5 Torr / Autoclave
3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 13 h / 0 - 20 °C / Inert atmosphere
With
copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); 5%-palladium/activated carbon; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1021/ja302574b