Technology Process of 2-ethenyl-N-3-butenyl-benzeneethaneamine
There total 5 articles about 2-ethenyl-N-3-butenyl-benzeneethaneamine 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:
-
but-3-en-1-amine hydrochloride; 2-(2-vinyl-phenyl)-ethylideneamine;
With
3-butene-1-amine;
In
diethyl ether; toluene;
at -15 - 20 ℃;
With
sodium cyanoborohydride;
In
diethyl ether; toluene;
at -15 - 20 ℃;
DOI:10.1016/j.tet.2003.08.071
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 80 percent / Pd(PPh3)4 / toluene / Heating
2.1: 100 percent / KOH / tetrahydrofuran / 4 h / 20 °C
3.1: 95 percent / acetonitrile / 20 °C
4.1: DIBALH / diethyl ether; toluene / -15 - 20 °C
5.1: homoallylamine / diethyl ether; toluene / -15 - 20 °C
5.2: NaCNBH3 / diethyl ether; toluene / -15 - 20 °C
With
potassium hydroxide; tetrakis(triphenylphosphine) palladium(0); 3-butene-1-amine; diisobutylaluminium hydride;
In
tetrahydrofuran; diethyl ether; toluene; acetonitrile;
1.1: Stille coupling;
DOI:10.1016/j.tet.2003.08.071
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 100 percent / KOH / tetrahydrofuran / 4 h / 20 °C
2.1: 95 percent / acetonitrile / 20 °C
3.1: DIBALH / diethyl ether; toluene / -15 - 20 °C
4.1: homoallylamine / diethyl ether; toluene / -15 - 20 °C
4.2: NaCNBH3 / diethyl ether; toluene / -15 - 20 °C
With
potassium hydroxide; 3-butene-1-amine; diisobutylaluminium hydride;
In
tetrahydrofuran; diethyl ether; toluene; acetonitrile;
DOI:10.1016/j.tet.2003.08.071
