HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl bromide → HCID 19990417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990467 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19990417 | HCID 19990417 | — |
Reaction Steps
To a solution of 0.3 g (1.1 mmol) 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline -2,3(1H,4H)-dione in 30 ml ethanol was added 0.7 ml triethylamine and 1.5 ml (12 mmol) cyclohexylbromide. The reaction mixture was refluxed for 7 days and then evaporated in vacuo. The residue was stirred with water to give a precipitate (0.25 g. Recrystallization (dimethylformamide-water) gave 0.17 g (44%) of 7-cyano-1-cyclohexyloxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione). M.p. 259° C. decomp. 1H-NMR (DMSO-d6): 8.0 (1H, s), 7.6 (1H, s), 4.3 (1H, m), 1.4 (8H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05061706 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-e6d29003c44d4356a642122cf4c5fa97 |
| Source note | uspto-grants-1991_10 |