Technology Process of C8H5BrClN
There total 3 articles about C8H5BrClN 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
tetrabutyl ammonium fluoride;
In
tetrahydrofuran;
at 20 ℃;
for 2h;
DOI:10.1055/s-0035-1561305
- Guidance literature:
-
Multi-step reaction with 3 steps
1: [bis(pyridine)iodine]+ tetrafluoroborate; tetrafluoroboric acid / dichloromethane / 20 °C
2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 6 h / 20 °C
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrafluoroboric acid; tetrabutyl ammonium fluoride; [bis(pyridine)iodine]+ tetrafluoroborate; triethylamine;
In
tetrahydrofuran; dichloromethane;
1: |Barluenga Lodination / 2: |Sonogashira Cross-Coupling;
DOI:10.1055/s-0035-1561305
- Guidance literature:
-
Multi-step reaction with 2 steps
1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 6 h / 20 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrabutyl ammonium fluoride; triethylamine;
In
tetrahydrofuran;
1: |Sonogashira Cross-Coupling;
DOI:10.1055/s-0035-1561305