Technology Process of C68H91ClN2O19
There total 1 articles about C68H91ClN2O19 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:
-
C60H85ClN2O17; 1,1'-carbonyldiimidazole;
With
potassium carbonate;
In
tetrahydrofuran;
at 20 ℃;
for 2h;
benzyl alcohol;
With
sodium hydride;
In
tetrahydrofuran;
at 20 ℃;
for 0.5h;
DOI:10.1016/j.bmc.2005.06.003
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 72 percent / NaH; MeI / 4.5 h / 60 °C
2: 63 percent / diethylaminosulfur trifluoride / CH2Cl2 / 72 h / 20 °C
3: 88 percent / hydrochloric acid / methanol / 1.5 h / 50 °C
4: 89 percent / DMSO; (CF3CO)2O; Et3N / CH2Cl2 / 1 h / -78 °C
With
hydrogenchloride; diethylamino-sulfur trifluoride; sodium hydride; dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride; methyl iodide;
In
methanol; dichloromethane;
DOI:10.1016/j.bmc.2005.06.003
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 72 percent / NaH; MeI / 4.5 h / 60 °C
2: 63 percent / diethylaminosulfur trifluoride / CH2Cl2 / 72 h / 20 °C
3: 88 percent / hydrochloric acid / methanol / 1.5 h / 50 °C
With
hydrogenchloride; diethylamino-sulfur trifluoride; sodium hydride; methyl iodide;
In
methanol; dichloromethane;
DOI:10.1016/j.bmc.2005.06.003