Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | HCID 12793832 | HCID 12793832 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19827814 | HCID 19827814 | 50% |
Reaction Steps
A solution of 2.0 g (8.4 mmol) N-cyclohexyl-4-fluoro-2-nitroaniline in a mixture of 100 ml ethanol and 50 ml ethyl acetate was hydrogenated at atm. pressure by using Ra-Ni (1 g) as a catalyst. The reaction mixture was filtered and evaporated in vacuo to give an oil. A mixture of the oil, 2.8 g (23 mmol) oxalic acid dihydrate, 10 ml ethanol and 150 ml 4N hydrochloric acid was refluxed for 11/2h. After cooling to 25° C. the precipitate was filtered off and washed with water to give 1.1 g (50%) 1-cyclohexyl-6-fluoroquinoxaline-2,3(1H,4H)-dione. M.p. 289.8° C., 1H-NMR (DMSO-d6): 12.0 (1H, broad s), 7.6 (1H, M), 7.0 (2H, M), 4.5 (1H, M), 2.6-0.9 (10H, M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05026704 |
|---|
| Source dataset | uspto-grants-1991_06 |
|---|
| ORD ID | ord-cde42b947da04dd3a9375fcd451c4319 |
|---|
| Source note | uspto-grants-1991_06 |
|---|