Technology Process of C19H24N2O3
There total 8 articles about C19H24N2O3 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
sodium acetate; dinitrogen tetraoxide;
In
dichloromethane;
at -30 ℃;
DOI:10.1021/jo01314a062
- Guidance literature:
-
Multi-step reaction with 8 steps
2: 1.) H2; 2.) p-TsOH / Pd/C / 1.)EtOH, 1 atm, 25 deg C; 2.) toluene, reflux
3: LiAlH4 / tetrahydrofuran / Heating
4: Et3N / CH2Cl2 / 0 °C
5: 77 percent / Et4NCl / dimethylsulfoxide / 72 h / 90 - 105 °C
6: 93 percent / LiAlH4 / diethyl ether / 0.5 h / 25 °C
7: 80 percent / pyridine / toluene / 70 °C
8: 97 percent / N2O4, NaOAc / CH2Cl2 / -30 °C
With
pyridine; lithium aluminium tetrahydride; tetraethylammonium chloride; hydrogen; sodium acetate; dinitrogen tetraoxide; toluene-4-sulfonic acid; triethylamine;
palladium on activated charcoal;
In
tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide; toluene;
DOI:10.1021/jo01314a062
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 1.) H2; 2.) p-TsOH / Pd/C / 1.)EtOH, 1 atm, 25 deg C; 2.) toluene, reflux
2: LiAlH4 / tetrahydrofuran / Heating
3: Et3N / CH2Cl2 / 0 °C
4: 77 percent / Et4NCl / dimethylsulfoxide / 72 h / 90 - 105 °C
5: 93 percent / LiAlH4 / diethyl ether / 0.5 h / 25 °C
6: 80 percent / pyridine / toluene / 70 °C
7: 97 percent / N2O4, NaOAc / CH2Cl2 / -30 °C
With
pyridine; lithium aluminium tetrahydride; tetraethylammonium chloride; hydrogen; sodium acetate; dinitrogen tetraoxide; toluene-4-sulfonic acid; triethylamine;
palladium on activated charcoal;
In
tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide; toluene;
DOI:10.1021/jo01314a062