Technology Process of C21H26NO2I
There total 7 articles about C21H26NO2I 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
1H-imidazole; iodine; triphenylphosphine;
In
benzene;
at 20 ℃;
for 1h;
DOI:10.1021/jo0708137
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 90 percent / CuI; triethylamine / PdCl2 / acetonitrile / 4 h / 20 °C
2: 85 percent / H2 / Pd/C / methanol / 48 h / 20 °C
3: 85 percent / NaHCO3 / dioxane; H2O / 12 h / 20 °C
4: 95 percent / imidazole / CH2Cl2 / 2 h / 20 °C
5: 90 percent / NaH / tetrahydrofuran / 12 h / Heating
6: 98 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h
7: I2; PPh3; imidazole / benzene / 1 h / 20 °C
With
1H-imidazole; copper(l) iodide; tetrabutyl ammonium fluoride; hydrogen; iodine; sodium hydride; sodium hydrogencarbonate; triethylamine; triphenylphosphine;
palladium on activated charcoal; palladium dichloride;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; acetonitrile; benzene;
DOI:10.1021/jo0708137
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 85 percent / H2 / Pd/C / methanol / 48 h / 20 °C
2: 85 percent / NaHCO3 / dioxane; H2O / 12 h / 20 °C
3: 95 percent / imidazole / CH2Cl2 / 2 h / 20 °C
4: 90 percent / NaH / tetrahydrofuran / 12 h / Heating
5: 98 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h
6: I2; PPh3; imidazole / benzene / 1 h / 20 °C
With
1H-imidazole; tetrabutyl ammonium fluoride; hydrogen; iodine; sodium hydride; sodium hydrogencarbonate; triphenylphosphine;
palladium on activated charcoal;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; benzene;
DOI:10.1021/jo0708137