Technology Process of C34H44N2O8
There total 8 articles about C34H44N2O8 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
diisobutylaluminium hydride;
In
tetrahydrofuran; toluene;
at -78 ℃;
for 1h;
Inert atmosphere;
DOI:10.1039/c3cc42365d
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: 1H-imidazole; triphenylphosphine; iodine / dichloromethane / 2 h / Cooling with ice; Inert atmosphere
2.1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / Cooling with ice; Inert atmosphere
2.2: 8 h / 20 °C / Inert atmosphere
2.3: 3.33 h / 20 °C / Inert atmosphere
3.1: C15H26Cl2CuN2O2; triethylamine / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere
4.1: Dess-Martin periodane / dichloromethane / 5 h / Cooling with ice; Inert atmosphere
5.1: dichloromethane / 15 h / 50 °C / Inert atmosphere
6.1: sodium hydrogencarbonate; mercuric triflate / dichloromethane / 10.5 h / -20 °C / Inert atmosphere; Cooling with ice
6.2: 0.5 h / -78 °C / Inert atmosphere
7.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / -78 °C / Inert atmosphere
With
1H-imidazole; C15H26Cl2CuN2O2; iodine; mercuric triflate; diisobutylaluminium hydride; sodium hydrogencarbonate; caesium carbonate; Dess-Martin periodane; triethylamine; triphenylphosphine;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene;
4.1: |Dess-Martin Oxidation / 5.1: |Wittig Olefination;
DOI:10.1039/c3cc42365d
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: C15H26Cl2CuN2O2; triethylamine / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere
2.1: Dess-Martin periodane / dichloromethane / 5 h / Cooling with ice; Inert atmosphere
3.1: dichloromethane / 15 h / 50 °C / Inert atmosphere
4.1: sodium hydrogencarbonate; mercuric triflate / dichloromethane / 10.5 h / -20 °C / Inert atmosphere; Cooling with ice
4.2: 0.5 h / -78 °C / Inert atmosphere
5.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / -78 °C / Inert atmosphere
With
C15H26Cl2CuN2O2; mercuric triflate; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; triethylamine;
In
tetrahydrofuran; dichloromethane; toluene;
2.1: |Dess-Martin Oxidation / 3.1: |Wittig Olefination;
DOI:10.1039/c3cc42365d