HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 8-Chloro-4-(4-methoxyphenyl)-3-oxoquinoxaline-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Des-(2-cyclohexane-1,3-dione) Fenquinotrione Ethyl Ester | HCID 67533339 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-Chloro-4-(4-methoxyphenyl)-3-oxoquinoxaline-2-carboxylic acid | HCID 67533290 | 94.2% |
Reaction Steps
7.7 g (21.5 mmol) of ethyl 5-chloro-1-(4-methoxyphenyl)-2-oxo-1,2-dihydroquinoxaline-3-carboxylate was dissolved in ethanol (100 ml), and 6.9 g (43.1 mmol) of a 25% aqueous solution of sodium hydroxide was added thereto. The mixture was stirred for 12 hours at room temperature. The reaction mixture was concentrated under reduced pressure, water was added to the residue thus obtained, and the mixture was acidified using 10% hydrochloric acid. A solid precipitated therefrom was separated by filtration, washed with water, and then dried, to obtain 6.7 g (yield: 94%) of 5-chloro-1-(4-methoxyphenyl)-2-oxo-1,2-dihydroquinoxaline-3-carboxylic acid as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648075B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-ebdf7b0fa55f45409467858eff7113dd |
| Source note | uspto-grants-2014_02 |