Technology Process of 3,11-dibromo-14-diphenylphosphoryldibenz[a,j]anthracene
There total 9 articles about 3,11-dibromo-14-diphenylphosphoryldibenz[a,j]anthracene 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
iodine;
In
tetrahydrofuran; diethyl ether;
at 20 ℃;
for 0.166667h;
Irradiation;
DOI:10.1016/j.tet.2012.12.048
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: toluene-4-sulfonic acid / acetone / Reflux
2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
2.2: 12 h / 20 °C
3.1: toluene-4-sulfonic acid / acetone / Reflux
4.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
4.2: 12 h / 20 °C
5.1: iodine / diethyl ether; tetrahydrofuran / 0.17 h / 20 °C / Irradiation
With
potassium tert-butylate; iodine; toluene-4-sulfonic acid;
In
tetrahydrofuran; diethyl ether; acetone;
2.2: |Wittig Olefination / 4.2: |Wittig Olefination;
DOI:10.1016/j.tet.2012.12.048
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: silver nitrate
2.1: toluene-4-sulfonic acid / toluene
3.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -80 °C
3.2: 0.5 h / -80 °C
4.1: toluene-4-sulfonic acid / acetone / Reflux
5.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
5.2: 12 h / 20 °C
6.1: toluene-4-sulfonic acid / acetone / Reflux
7.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
7.2: 12 h / 20 °C
8.1: iodine / diethyl ether; tetrahydrofuran / 0.17 h / 20 °C / Irradiation
With
n-butyllithium; potassium tert-butylate; iodine; toluene-4-sulfonic acid; silver nitrate;
In
tetrahydrofuran; diethyl ether; hexane; acetone; toluene;
5.2: |Wittig Olefination / 7.2: |Wittig Olefination;
DOI:10.1016/j.tet.2012.12.048