Technology Process of 2-bromo-9,9-dioctyl-7-(4-(1,2,2-triphenylethylenyl)phenyl)-9H-fluorene
There total 7 articles about 2-bromo-9,9-dioctyl-7-(4-(1,2,2-triphenylethylenyl)phenyl)-9H-fluorene 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
tetrakis(triphenylphosphine) palladium(0); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate;
In
water; toluene;
at 90 ℃;
for 20h;
Inert atmosphere;
DOI:10.1039/c2jm30261f
- Guidance literature:
-
Multi-step reaction with 3 steps
1: potassium iodate; iodine / water; acetic acid / 2 h / 90 °C / Inert atmosphere
2: sodium hydroxide / water; dimethyl sulfoxide / 24 h / Inert atmosphere
3: tetrakis(triphenylphosphine) palladium(0); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / water; toluene / 20 h / 90 °C / Inert atmosphere
With
potassium iodate; tetrakis(triphenylphosphine) palladium(0); iodine; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; sodium hydroxide;
In
water; acetic acid; dimethyl sulfoxide; toluene;
DOI:10.1039/c2jm30261f
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: toluene-4-sulfonic acid / toluene / 6 h / Reflux
2.1: n-butyllithium / tetrahydrofuran; hexane / 3 h / -78 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
2.3: 1 h
3.1: tetrakis(triphenylphosphine) palladium(0); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / water; toluene / 20 h / 90 °C / Inert atmosphere
With
tetrakis(triphenylphosphine) palladium(0); n-butyllithium; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; toluene-4-sulfonic acid;
In
tetrahydrofuran; hexane; water; toluene;
DOI:10.1039/c2jm30261f