Technology Process of C15H18O4
There total 7 articles about C15H18O4 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:
-
C15H20O5;
With
pyridine; trifluoromethylsulfonic anhydride;
In
dichloromethane;
at -78 - 0 ℃;
Inert atmosphere;
With
1,8-diazabicyclo[5.4.0]undec-7-ene;
In
dichloromethane;
at 20 ℃;
for 2h;
Inert atmosphere;
DOI:10.1021/ja107190w
- Guidance literature:
-
With
1,8-diazabicyclo[5.4.0]undec-7-ene;
In
dichloromethane;
at 20 ℃;
for 2h;
Inert atmosphere;
DOI:10.1021/ja2041964
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: potassium hexacyanoferrate (III); (DHQD)2PHAL; potassium osmate; methanesulfonamide; potassium carbonate / water; tert-butyl alcohol / 0 °C / Inert atmosphere
1.2: 0.67 h / 20 °C / Inert atmosphere
2.1: pyridinium p-toluenesulfonate / acetone / 1 h / 20 °C / Inert atmosphere
3.1: pyridine / dichloromethane / -78 - 0 °C / Inert atmosphere
4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 20 °C / Inert atmosphere
With
pyridine; potassium hexacyanoferrate (III); (DHQD)2PHAL; potassium osmate; methanesulfonamide; pyridinium p-toluenesulfonate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
dichloromethane; water; acetone; tert-butyl alcohol;
1.1: Sharpless dihydroxylation;
DOI:10.1021/ja2041964