Technology Process of C30H35N6O8S(3-)*Gd(3+)
There total 9 articles about C30H35N6O8S(3-)*Gd(3+) 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
gadolinium(III) chloride; sodium hydroxide;
In
water;
at 59.84 ℃;
for 24h;
pH=7;
DOI:10.1021/ml400042w
- Guidance literature:
-
Multi-step reaction with 2 steps
1: trifluoroacetic acid / dichloromethane / 45 °C
2: sodium hydroxide; gadolinium(III) chloride / water / 24 h / 59.84 °C / pH 7
With
gadolinium(III) chloride; trifluoroacetic acid; sodium hydroxide;
In
dichloromethane; water;
DOI:10.1021/ml400042w
- Guidance literature:
-
Multi-step reaction with 8 steps
1: triethylamine / tetrahydrofuran / 2 h / 0 - 20 °C
2: Lawessons reagent / chlorobenzene / 4 h / Reflux
3: sodium hydroxide / water; ethanol / 3 h / Reflux
4: tin(ll) chloride / ethanol / 4 h / Reflux
5: potassium carbonate / acetonitrile / 2 h
6: potassium carbonate / acetonitrile / 48 h / 20 °C
7: trifluoroacetic acid / dichloromethane / 45 °C
8: sodium hydroxide; gadolinium(III) chloride / water / 24 h / 59.84 °C / pH 7
With
Lawessons reagent; gadolinium(III) chloride; potassium carbonate; triethylamine; trifluoroacetic acid; tin(ll) chloride; sodium hydroxide;
In
tetrahydrofuran; ethanol; dichloromethane; water; chlorobenzene; acetonitrile;
DOI:10.1021/ml400042w