Technology Process of C34H27N3O7
There total 5 articles about C34H27N3O7 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
triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
DOI:10.1021/jf4011033
-
-
477-51-0,6258-33-9,17187-81-4,17301-90-5,19186-35-7,24150-39-8,31892-96-3,55568-81-5,64550-41-0,69222-20-4,75171-57-2,83023-41-0,100348-38-7
deoxypodophyllotoxin
- Guidance literature:
-
Multi-step reaction with 4 steps
1: nitric acid; propionic acid / 0.07 h / 0 °C
2: chloroform / 5 h / 20 °C
3: tin(II) chloride dihdyrate / ethyl acetate / 7 h / Inert atmosphere; Reflux
4: triethylamine / dichloromethane / 0 - 20 °C
With
tin(II) chloride dihdyrate; nitric acid; propionic acid; triethylamine;
In
dichloromethane; chloroform; ethyl acetate;
DOI:10.1021/jf4011033
- Guidance literature:
-
Multi-step reaction with 5 steps
1: hydrogen; palladium 10% on activated carbon; acetic acid / 5 h / 95 °C / 1520.1 Torr
2: nitric acid; propionic acid / 0.07 h / 0 °C
3: chloroform / 5 h / 20 °C
4: tin(II) chloride dihdyrate / ethyl acetate / 7 h / Inert atmosphere; Reflux
5: triethylamine / dichloromethane / 0 - 20 °C
With
tin(II) chloride dihdyrate; palladium 10% on activated carbon; hydrogen; nitric acid; acetic acid; propionic acid; triethylamine;
In
dichloromethane; chloroform; ethyl acetate;
DOI:10.1021/jf4011033