HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5,6,7-Trifluoro-1,4-dihydro-2,3-quinoxalinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | 3,4,5-Trifluorobenzene-1,2-diamine | HCID 2773958 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5,6,7-Trifluoro-1,4-dihydro-2,3-quinoxalinedione | HCID 10846370 | 36% |
Reaction Steps
To a brown solution of 3,4,5-trifluoro-1,2-phenylenediamine (285 mg, 1.75 mmol) in aqueous 2N HCl (10 mL) is added oxalic acid (221 mg, 1.75 mmol). The brown mixture is brought to reflux and stirred under N2 overnight. The mixture is filtered to yield 139 mg (37%) of crude title compound. An analytical sample is prepared by dissolving 42 mg of this brown powder in 2.5 mL boiling ethanol. Upon cooling, brown rod-like crystals were formed which are filtered and dried in vacuo to yield 15 mg (36%) of pure title compound: 1H NMR (DMSO-d6), 6.91 (m, 1H), 12.02 (s, 1H), 12.19 (s, 1H); analysis calculated for C8H3F3N2O2 : C, 44.46; H, 1.40; N, 12.96. Found: C, 44.42; H, 1.16; N, 12.76.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620979 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-9050ce0a21ba412fbe55497e968b965f |
| Source note | uspto-grants-1997_04 |