Technology Process of 2-phenylpenta-3,4-dien-2-amine
There total 6 articles about 2-phenylpenta-3,4-dien-2-amine 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:
-
trans-3-ethynyl-2-methyl-2-phenylaziridine;
With
9-bora-bicyclo[3.3.1]nonane;
In
tetrahydrofuran;
at 0 - 25 ℃;
Inert atmosphere;
With
dihydrogen peroxide; sodium hydroxide;
In
tetrahydrofuran; water;
at 0 - 20 ℃;
Inert atmosphere;
DOI:10.1002/anie.200906066
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: triphenylphosphine / acetonitrile / 50 - 83 °C
2.1: diisobutylaluminium hydride / toluene / -78 °C
3.1: potassium carbonate / methanol / 8 h / 20 °C / Inert atmosphere
4.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
4.2: 0 - 20 °C / Inert atmosphere
With
diisobutylaluminium hydride; potassium carbonate; 9-bora-bicyclo[3.3.1]nonane; triphenylphosphine;
In
tetrahydrofuran; methanol; toluene; acetonitrile;
3.1: Wittig-type reaction;
DOI:10.1002/anie.200906066
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: sodium azide; ammonium chloride / ethanol / 8 h / 80 °C
2.1: triphenylphosphine / acetonitrile / 50 - 83 °C
3.1: diisobutylaluminium hydride / toluene / -78 °C
4.1: potassium carbonate / methanol / 8 h / 20 °C / Inert atmosphere
5.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
5.2: 0 - 20 °C / Inert atmosphere
With
sodium azide; diisobutylaluminium hydride; potassium carbonate; ammonium chloride; 9-bora-bicyclo[3.3.1]nonane; triphenylphosphine;
In
tetrahydrofuran; methanol; ethanol; toluene; acetonitrile;
4.1: Wittig-type reaction;
DOI:10.1002/anie.200906066