Technology Process of C35H60Cl2N2O2
There total 10 articles about C35H60Cl2N2O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C / Inert atmosphere
1.2: -78 - 20 °C / Inert atmosphere
2.1: hydrogenchloride / methanol; water / 124 h / 20 °C / Inert atmosphere
3.1: sulfuric acid / 18 h / Inert atmosphere; Heating
3.2: 0 °C / Inert atmosphere
4.1: 20 % Pd(OH)2/C; hydrogen / methanol / 16 h / 70 °C / 4137.29 Torr
5.1: hydrogenchloride; water / ethanol / 20 h / Inert atmosphere; Reflux
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 13 h / 0 °C / Inert atmosphere; Reflux
6.2: 0.5 h / 0 °C / Inert atmosphere; Reflux
7.1: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere
8.1: thionyl chloride / toluene / 3 h / Inert atmosphere; Reflux
With
hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; oxalyl dichloride; sulfuric acid; 20 % Pd(OH)2/C; water; hydrogen; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene;
DOI:10.1016/j.tet.2011.02.027
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 13 h / 0 °C / Inert atmosphere; Reflux
1.2: 0.5 h / 0 °C / Inert atmosphere; Reflux
2.1: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere
3.1: thionyl chloride / toluene / 3 h / Inert atmosphere; Reflux
With
lithium aluminium tetrahydride; thionyl chloride; triethylamine;
In
tetrahydrofuran; dichloromethane; toluene;
DOI:10.1016/j.tet.2011.02.027