HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Diethyl 2-oxopropanedioate → Ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Diethyl 2-oxopropanedioate | HCID 69105 | — |
| Reactant | (2-Amino-3-chlorophenyl)amine | HCID 3462489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate | HCID 67531483 | 56.5% |
Reaction Steps
10.5 g (73.6 mmol) of 3-chloro-1,2-phenylenediamine and 12.8 g (73.5 mmol) of diethyl ketomalonate were dissolved in ethanol, and the solution was heated to reflux for 3 hours. While heating to reflux, ethanol was added thereto until precipitated crystals dissolved. The reaction mixture was cooled to room temperature, and then precipitated crystals were separated by filtration. The filter cake was washed with cold ethanol, and then dried, to obtain 10.5 g (yield: 51%) of ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate as pale yellow acicular crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389523B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-e4dd8dab326b47cd84951be91ddabc2e |
| Source note | uspto-grants-2013_03 |