Technology Process of Benzenemethanamine, N-methyl-N-phenyl-, hydrochloride
There total 3 articles about Benzenemethanamine, N-methyl-N-phenyl-, hydrochloride 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:
-
N-methyl-N-phenyl-benzamide;
With
[κ2-{Ph2P(Se)NC9H6N}Al(Me)2]; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane;
at 20 ℃;
for 12h;
Schlenk technique;
Glovebox;
With
hydrogenchloride;
In
water;
chemoselective reaction;
DOI:10.1039/c9dt01806a
- Guidance literature:
-
With
hydrogen; tris(2,6-difluorophenyl)borane triethylphosphine oxide;
In
chloroform;
at 40 ℃;
for 48h;
under 60006 Torr;
Autoclave;
DOI:10.1021/jacs.8b12997
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0 °C / Inert atmosphere
1.2: 2 h / 0 - 20 °C / Inert atmosphere
2.1: tris(2,6-difluorophenyl)borane triethylphosphine oxide; oxalyl dichloride / chloroform / Sealed tube; Inert atmosphere; Glovebox
3.1: hydrogen; tris(2,6-difluorophenyl)borane triethylphosphine oxide / chloroform / 48 h / 40 °C / 60006 Torr / Autoclave
With
oxalyl dichloride; hydrogen; sodium hydride; tris(2,6-difluorophenyl)borane triethylphosphine oxide;
In
tetrahydrofuran; chloroform; mineral oil;
DOI:10.1021/jacs.8b12997