Technology Process of C16H9ClFNO5S
There total 4 articles about C16H9ClFNO5S 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
trifluoroacetic acid;
In
dichloromethane; water;
at 20 ℃;
for 0.5h;
DOI:10.1016/j.ab.2011.03.008
- Guidance literature:
-
Multi-step reaction with 2 steps
1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; potassium carbonate / acetonitrile / 2 h / 50 °C
2: trifluoroacetic acid / dichloromethane; water / 0.5 h / 20 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate; trifluoroacetic acid;
In
dichloromethane; water; acetonitrile;
DOI:10.1016/j.ab.2011.03.008
- Guidance literature:
-
Multi-step reaction with 3 steps
1: phosphorus trichloride / 5,5-dimethyl-1,3-cyclohexadiene / 1 h / Reflux
2: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; potassium carbonate / acetonitrile / 2 h / 50 °C
3: trifluoroacetic acid / dichloromethane; water / 0.5 h / 20 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate; trifluoroacetic acid; phosphorus trichloride;
In
5,5-dimethyl-1,3-cyclohexadiene; dichloromethane; water; acetonitrile;
DOI:10.1016/j.ab.2011.03.008
