HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Ethyl 4-ethyl-6-fluoro-3,4-dihydro-3-oxo-2-quinoxalinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10752268 | HCID 10752268 | — |
| Reactant | HCID 10823684 | HCID 10823684 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Ethyl 4-ethyl-6-fluoro-3,4-dihydro-3-oxo-2-quinoxalinecarboxylate | HCID 86734255 | — |
Reaction Steps
The mixture of 6-fluoro-3,4-dihydro-3-oxo-2-quinoxalinecarboxylic acid, ethyl ester and 7-fluoro-3,4-dihydro-3-oxo-2-quinoxalinecarboxylic acid, ethyl ester (Example 22a) (2 g), ethyl iodide (4 g) and anhydrous potassium carbonate (5.9 g) in 2-butanone (200 ml) were heated under reflux for 5 hours. The mixture was filtered and the filtrate was evaporated. The residual oil was chromatographed on silica using a mixture of petroleum ether (b.p. 60°-80°) and ethyl acetate (3:1) as eluent to give the required product, on evaporation of the later fractions, m.p. 99°-101.5°, (50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997535 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-7dd95d4a2a0b42f9b8a0209babd1e711 |
| Source note | uspto-grants-1976_12 |