Technology Process of C22H20N2O6
There total 8 articles about C22H20N2O6 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
(cyclooctadienyl)(cyclopentadienyl)ruthenium chloride;
In
1,2-dichloro-ethane;
at -78 - 20 ℃;
DOI:10.1016/j.tetlet.2011.06.100
- Guidance literature:
-
Multi-step reaction with 5 steps
1: water; acetic acid / 2 h / Reflux
2: dmap; triethylamine / dichloromethane / 1 h / 20 °C
3: N,O-bis-(trimethylsilyl)-acetamide; trimethylsilyl trifluoromethanesulfonate / acetonitrile / 2 h / 50 °C
4: methanol; sodium methylate / 0.33 h / 20 °C
5: (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride / 1,2-dichloro-ethane / -78 - 20 °C
With
methanol; dmap; N,O-bis-(trimethylsilyl)-acetamide; (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride; trimethylsilyl trifluoromethanesulfonate; water; sodium methylate; acetic acid; triethylamine;
In
dichloromethane; 1,2-dichloro-ethane; acetonitrile;
4: Zemplen deacetylation;
DOI:10.1016/j.tetlet.2011.06.100
- Guidance literature:
-
Multi-step reaction with 3 steps
1: N,O-bis-(trimethylsilyl)-acetamide; trimethylsilyl trifluoromethanesulfonate / acetonitrile / 2 h / 50 °C
2: methanol; sodium methylate / 0.33 h / 20 °C
3: (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride / 1,2-dichloro-ethane / -78 - 20 °C
With
methanol; N,O-bis-(trimethylsilyl)-acetamide; (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride; trimethylsilyl trifluoromethanesulfonate; sodium methylate;
In
1,2-dichloro-ethane; acetonitrile;
2: Zemplen deacetylation;
DOI:10.1016/j.tetlet.2011.06.100