Technology Process of CF3O3S(1-)*C33H25N2O2(1+)
There total 12 articles about CF3O3S(1-)*C33H25N2O2(1+) 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:
-
Multi-step reaction with 9 steps
1.1: sodium tetrahydroborate / methanol / 1 h / 0 - 20 °C
2.1: Amberlyst 15 / hexane / 3 h / 0 - 20 °C / Reflux
3.1: C38H42ClMnN2O4; 4-methylmorpholine N-oxide / dichloromethane / 0.25 h / -78 °C
3.2: -78 °C
4.1: sodium azide; ammonium chloride / ethanol; water / 2 h / Reflux
5.1: palladium 10% on activated carbon; hydrogen / methanol / 0.33 h
6.1: acetic acid / tetrahydrofuran / 16 h / 90 °C
7.1: thionyl chloride / toluene / 16 h / 90 °C
8.1: sodium hydroxide / tetrahydrofuran; ethanol / 3 h / 90 °C
9.1: dichloromethane / 2 h / 20 °C / Darkness
With
sodium tetrahydroborate; thionyl chloride; sodium azide; palladium 10% on activated carbon; C38H42ClMnN2O4; hydrogen; ammonium chloride; acetic acid; 4-methylmorpholine N-oxide; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; water; toluene;
DOI:10.1039/c1ob06780j
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: tetrakis(triphenylphosphine) palladium(0); sodium carbonate / tetrahydrofuran; water / Inert atmosphere; Reflux
2.1: sodium tetrahydroborate / methanol / 1 h / 0 - 20 °C
3.1: Amberlyst 15 / hexane / 3 h / 0 - 20 °C / Reflux
4.1: C38H42ClMnN2O4; 4-methylmorpholine N-oxide / dichloromethane / 0.25 h / -78 °C
4.2: -78 °C
5.1: sodium azide; ammonium chloride / ethanol; water / 2 h / Reflux
6.1: palladium 10% on activated carbon; hydrogen / methanol / 0.33 h
7.1: acetic acid / tetrahydrofuran / 16 h / 90 °C
8.1: thionyl chloride / toluene / 16 h / 90 °C
9.1: sodium hydroxide / tetrahydrofuran; ethanol / 3 h / 90 °C
10.1: dichloromethane / 2 h / 20 °C / Darkness
With
sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium(0); thionyl chloride; sodium azide; palladium 10% on activated carbon; C38H42ClMnN2O4; hydrogen; sodium carbonate; ammonium chloride; acetic acid; 4-methylmorpholine N-oxide; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; water; toluene;
DOI:10.1039/c1ob06780j
- Guidance literature:
-
Multi-step reaction with 11 steps
1.1: triethylamine / dichloromethane / 24 h / 20 °C
2.1: tetrakis(triphenylphosphine) palladium(0); sodium carbonate / tetrahydrofuran; water / Inert atmosphere; Reflux
3.1: sodium tetrahydroborate / methanol / 1 h / 0 - 20 °C
4.1: Amberlyst 15 / hexane / 3 h / 0 - 20 °C / Reflux
5.1: C38H42ClMnN2O4; 4-methylmorpholine N-oxide / dichloromethane / 0.25 h / -78 °C
5.2: -78 °C
6.1: sodium azide; ammonium chloride / ethanol; water / 2 h / Reflux
7.1: palladium 10% on activated carbon; hydrogen / methanol / 0.33 h
8.1: acetic acid / tetrahydrofuran / 16 h / 90 °C
9.1: thionyl chloride / toluene / 16 h / 90 °C
10.1: sodium hydroxide / tetrahydrofuran; ethanol / 3 h / 90 °C
11.1: dichloromethane / 2 h / 20 °C / Darkness
With
sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium(0); thionyl chloride; sodium azide; palladium 10% on activated carbon; C38H42ClMnN2O4; hydrogen; sodium carbonate; ammonium chloride; acetic acid; 4-methylmorpholine N-oxide; triethylamine; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; water; toluene;
DOI:10.1039/c1ob06780j