HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346170Generated: October 30, 2026
Hydrochloric Acid → 1-carboxymethyloxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione
https://huagongshe.com/reaction/346170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990467 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-carboxymethyloxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990439 | 74.6% |
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 30 ml 0.5M phosphate buffer pH 7.4. The mixture was added 0.9 g (6.5 mmol) bromoacetic acid and then stirred at 25° C. for 10 days. 4N hydrochloric acid was added to pH 1, and then the reaction mixture was evaporated in vacuo. The residue was stirred with water to give 0.27 g (74%) of 1-carboxymethyloxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione. M.p. 257° C. 1H-NMR (DMSO-d6): 8.2 (1H, s), 7.6 (1H, s), 4.8 (2H, 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-2fcd0c9acece4741b78aaafaeafb5537 |
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| Source note | uspto-grants-1991_10 |
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