HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942152Generated: October 26, 2026
Pyridine → Des-(2-cyclohexane-1,3-dione) Fenquinotrione Ethyl Ester
https://huagongshe.com/reaction/1942152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxyphenyl boric acid | HCID 14769994 | — |
| Reactant | Ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate | HCID 67531483 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Des-(2-cyclohexane-1,3-dione) Fenquinotrione Ethyl Ester | HCID 67533339 | 78% |
Reaction Steps
To a slurry containing 5.7 g (22.6 mmol) of ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate, 6.9 g (45.4 mmol) of 4-methoxyphenylboric acid, 8.2 g (45.1 mmol) of anhydrous copper (II) acetate and chloroform (200 ml), 3.6 g (45.5 mmol) of pyridine and 4.6 g (45.5 mmol) of triethylamine were added dropwise, and the mixture was stirred for 72 hours at room temperature. The reaction mixture was washed with 10% hydrochloric acid, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was isolated by silica gel chromatography (developing solvent: ethyl acetate:hexane=2:3), and the isolated solid was washed with diisopropyl ether, to obtain 6.3 g (yield: 78%) of ethyl 5-chloro-1-(4-methoxyphenyl)-2-oxo-1,2-dihydroquinoxaline-3-carboxylate as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389523B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-090bc26c1a3542409874de63f2997b9f |
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| Source note | uspto-grants-2013_03 |
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