Technology Process of N-butyl-2-bromo-4-methylaniline
There total 7 articles about N-butyl-2-bromo-4-methylaniline 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
[Ru(bpyrz)3](PF6)2*2H2O;
In
methanol; acetonitrile;
at 20 ℃;
for 15h;
Air;
Visible light;
Irradiation;
DOI:10.1055/s-0030-1260082
- Guidance literature:
-
Multi-step reaction with 4 steps
1: pyridine; N-Bromosuccinimide / dichloromethane / 0.5 h / 0 °C / Inert atmosphere
2: tetrahydrofuran / 0.25 h / -100 °C / Inert atmosphere
3: trifluoroacetic acid / dichloromethane / 0 °C / Inert atmosphere
4: [Ru(bpyrz)3](PF6)2*2H2O / methanol; acetonitrile / 15 h / 20 °C / Air; Visible light; Irradiation
With
pyridine; N-Bromosuccinimide; [Ru(bpyrz)3](PF6)2*2H2O; trifluoroacetic acid;
In
tetrahydrofuran; methanol; dichloromethane; acetonitrile;
DOI:10.1055/s-0030-1260082
- Guidance literature:
-
Multi-step reaction with 3 steps
1: tetrahydrofuran / 0.25 h / -100 °C / Inert atmosphere
2: trifluoroacetic acid / dichloromethane / 0 °C / Inert atmosphere
3: [Ru(bpyrz)3](PF6)2*2H2O / methanol; acetonitrile / 15 h / 20 °C / Air; Visible light; Irradiation
With
[Ru(bpyrz)3](PF6)2*2H2O; trifluoroacetic acid;
In
tetrahydrofuran; methanol; dichloromethane; acetonitrile;
DOI:10.1055/s-0030-1260082