Technology Process of C13H15IO3
There total 10 articles about C13H15IO3 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
sodium hydrogencarbonate; Dess-Martin periodane;
In
dichloromethane;
for 1.5h;
DOI:10.1016/j.tet.2011.07.066
- Guidance literature:
-
Multi-step reaction with 4 steps
1: potassium carbonate / methanol / 1.17 h / 0 - 20 °C
2: tetrakis(triphenylphosphine) palladium(0); tri-n-butyl-tin hydride / tetrahydrofuran / 0.33 h
3: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 °C
4: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 1.5 h
With
tetrakis(triphenylphosphine) palladium(0); tri-n-butyl-tin hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane;
In
tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1016/j.tet.2011.07.066
- Guidance literature:
-
Multi-step reaction with 5 steps
1: sulfur trioxide pyridine complex; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 0 °C
2: potassium carbonate / methanol / 1.17 h / 0 - 20 °C
3: tetrakis(triphenylphosphine) palladium(0); tri-n-butyl-tin hydride / tetrahydrofuran / 0.33 h
4: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 °C
5: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 1.5 h
With
tetrakis(triphenylphosphine) palladium(0); tri-n-butyl-tin hydride; sulfur trioxide pyridine complex; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1016/j.tet.2011.07.066