HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyloxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19990467 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Monobasic potassium phosphate | HCID 516951 | — |
| Product | 1-Benzyloxy-7-cyano-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione | HCID 19421405 | 75% |
Reaction Steps
To a solution of 10.0 g (~36.9 mmol) of 7-cyano-1-hydroxy-6-trifluoromethylquinoxaline-2,3(1H,4H)-dione in a mixture of 700 ml of ethanol and 175 ml of 1M potassium dihydrogen phosphate buffer pH 7.4 was added 14 g (~81 mmol) of benzylbromide. Stirring was continued for 2 h at 25° C. The precipitate was filtered off and washed with ice-cold ethanol to give the title compound (9.9 g; 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559106 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-b90f781ab93444328cb8bf81827d8e1d |
| Source note | uspto-grants-1996_09 |