Technology Process of C8H10N2O2
There total 5 articles about C8H10N2O2 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
ammonium cerium (IV) nitrate; water;
In
acetonitrile;
at 0 ℃;
for 0.5h;
DOI:10.1002/chem.201201192
- Guidance literature:
-
Multi-step reaction with 5 steps
1: sodium acetate / ethanol / 24 h / 20 °C / Inert atmosphere
2: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / Reflux; Inert atmosphere
3: titanium tetrachloride; triethylamine / toluene / 12 h / 0 - 20 °C / Inert atmosphere
4: (R)-N-(phenylcarbamoyl)-tert-butanesulfinamide; trichlorosilane; water / acetonitrile / 24 h / -40 °C
5: ammonium cerium (IV) nitrate; water / acetonitrile / 0.5 h / 0 °C
With
ammonium cerium (IV) nitrate; (R)-N-(phenylcarbamoyl)-tert-butanesulfinamide; trichlorosilane; water; sodium acetate; titanium tetrachloride; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
ethanol; ethyl acetate; toluene; acetonitrile;
DOI:10.1002/chem.201201192
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / Reflux; Inert atmosphere
2: titanium tetrachloride; triethylamine / toluene / 12 h / 0 - 20 °C / Inert atmosphere
3: (R)-N-(phenylcarbamoyl)-tert-butanesulfinamide; trichlorosilane; water / acetonitrile / 24 h / -40 °C
4: ammonium cerium (IV) nitrate; water / acetonitrile / 0.5 h / 0 °C
With
ammonium cerium (IV) nitrate; (R)-N-(phenylcarbamoyl)-tert-butanesulfinamide; trichlorosilane; water; titanium tetrachloride; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
ethyl acetate; toluene; acetonitrile;
DOI:10.1002/chem.201201192