Technology Process of C18H26FNO4
There total 4 articles about C18H26FNO4 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
(bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
dichloromethane;
at -78 - 20 ℃;
DOI:10.1016/j.bmcl.2010.12.078
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: formic acid; di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / Reflux
1.2: 20 °C
2.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / -78 - 20 °C
With
formic acid; di-isopropyl azodicarboxylate; triphenylphosphine; (bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
tetrahydrofuran; dichloromethane;
1.1: Mitsunobu reaction / 1.2: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2010.12.078
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C
2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C
3.1: formic acid; di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / Reflux
3.2: 20 °C
4.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / -78 - 20 °C
With
lithium borohydride; formic acid; di-isopropyl azodicarboxylate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; (bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
tetrahydrofuran; dichloromethane;
3.1: Mitsunobu reaction / 3.2: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2010.12.078