HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346140Generated: October 29, 2026
Triethylamine → 7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dione
https://huagongshe.com/reaction/346140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dione | HCID 19990466 | 83% |
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 0.225 ml (1.63 mmol) dry triethylamine and 0.2 ml (1.58 mmol) phenyl chloroformate. The mixture was stirred at 25° C. for 30 min., and then filtered and evaporated in vacuo. The residue was stirred with ether to give 0.48 g (83%) of 7-cyano-1-phenoxycarbonyloxy-6-trifluoromethylquinoxaline-2,3-(1H,4H)-dione. M.p. 190° C. decomp. 1H-NMR (DMSO-d6): 8.43 (1H,s), 7.63 (1H, s), 7.3 (5H, broad s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05061706 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-fb0a15971e8e430dad4603c3a94073fb |
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| Source note | uspto-grants-1991_10 |
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