HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-acetoxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-acetoxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990412 | 92% |
Reaction Steps
A solution of 0.4 g (1.48 mmol) 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione in 50 ml dry tetrahydrofuran was added 0.3 ml (2.18 mmol) dry triethylamine and 0.15 ml (2.10 mmol) acetyl chloride. The mixture was refluxed for 3 h, and then evaporated in vacuo. The residue was stirred with water to give 0.42 g (92%) of 1-acetoxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione. M.p. 230° C. 1H-NMR (DMSO-d6): 8.16 (1H, s), 7.53 (1H, s), 2.37 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05061706 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-8ffd17ef78204d8e877df1910aa90bf3 |
| Source note | uspto-grants-1991_10 |