Technology Process of 1-bromo-4-fluoro-2-(2-iodophenoxy)benzene
There total 4 articles about 1-bromo-4-fluoro-2-(2-iodophenoxy)benzene 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
toluene-4-sulfonic acid; potassium iodide; sodium nitrite;
In
water; acetonitrile;
at 5 - 20 ℃;
Inert atmosphere;
DOI:10.1002/chem.201003559
- Guidance literature:
-
Multi-step reaction with 2 steps
1: hydrogenchloride; acetic acid; zinc / ethyl acetate / 0 °C / Inert atmosphere
2: toluene-4-sulfonic acid; potassium iodide; sodium nitrite / water; acetonitrile / 5 - 20 °C / Inert atmosphere
With
hydrogenchloride; toluene-4-sulfonic acid; acetic acid; potassium iodide; zinc; sodium nitrite;
In
water; ethyl acetate; acetonitrile;
DOI:10.1002/chem.201003559
- Guidance literature:
-
Multi-step reaction with 3 steps
1: potassium carbonate / dimethyl sulfoxide / 22 h / 95 °C / Inert atmosphere
2: hydrogenchloride; acetic acid; zinc / ethyl acetate / 0 °C / Inert atmosphere
3: toluene-4-sulfonic acid; potassium iodide; sodium nitrite / water; acetonitrile / 5 - 20 °C / Inert atmosphere
With
hydrogenchloride; potassium carbonate; toluene-4-sulfonic acid; acetic acid; potassium iodide; zinc; sodium nitrite;
In
water; dimethyl sulfoxide; ethyl acetate; acetonitrile;
DOI:10.1002/chem.201003559