Technology Process of C26H34N2O4
There total 7 articles about C26H34N2O4 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:
-
Multi-step reaction with 3 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / Inert atmosphere
2: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 - 20 °C / Inert atmosphere
3: methanol / Inert atmosphere
With
oxalyl dichloride; tetrabutyl ammonium fluoride; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja207591e
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 2-nitrobenzenesulfonyl hydrazide; triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / -15 - 20 °C / Inert atmosphere
2: tetrabutyl ammonium fluoride / tetrahydrofuran / Inert atmosphere
3: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 - 20 °C / Inert atmosphere
4: methanol / Inert atmosphere
With
oxalyl dichloride; 2-nitrobenzenesulfonyl hydrazide; tetrabutyl ammonium fluoride; dimethyl sulfoxide; triethylamine; triphenylphosphine; diethylazodicarboxylate;
In
tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja207591e
- Guidance literature:
-
Multi-step reaction with 2 steps
1: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 - 20 °C / Inert atmosphere
2: methanol / Inert atmosphere
With
oxalyl dichloride; dimethyl sulfoxide; triethylamine;
In
methanol; dichloromethane;
DOI:10.1021/ja207591e