Technology Process of C33H37NO4
There total 9 articles about C33H37NO4 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
chlorosulfonic acid;
In
dichloromethane;
at -30 ℃;
for 6h;
DOI:10.1021/ol301331t
- Guidance literature:
-
Multi-step reaction with 5 steps
1: water; toluene-4-sulfonic acid / acetone / 24 h / 70 °C
2: potassium hydroxide / dimethyl sulfoxide / 2 h / 25 °C / Inert atmosphere
3: sodium tetrahydroborate / ethanol / 2 h / 25 °C
4: pyridine; 3-chloro-benzenecarboperoxoic acid / hexane; dichloromethane / -30 - 20 °C
5: chlorosulfonic acid / dichloromethane / 6 h / -30 °C
With
pyridine; chlorosulfonic acid; sodium tetrahydroborate; water; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide;
In
ethanol; hexane; dichloromethane; dimethyl sulfoxide; acetone;
5: Schmidt reaction;
DOI:10.1021/ol301331t
- Guidance literature:
-
Multi-step reaction with 3 steps
1: sodium tetrahydroborate / ethanol / 2 h / 25 °C
2: pyridine; 3-chloro-benzenecarboperoxoic acid / hexane; dichloromethane / -30 - 20 °C
3: chlorosulfonic acid / dichloromethane / 6 h / -30 °C
With
pyridine; chlorosulfonic acid; sodium tetrahydroborate; 3-chloro-benzenecarboperoxoic acid;
In
ethanol; hexane; dichloromethane;
3: Schmidt reaction;
DOI:10.1021/ol301331t