HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254031Generated: October 26, 2026
Water → 2-Cyano-2-methyl-4-[4-(6-trifluoromethyl-2-quinoxalinyloxy)-phenoxy]-3-butanone
https://huagongshe.com/reaction/2254031
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-6-(trifluoromethyl)quinoxaline | HCID 3547342 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 2-Cyano-2-methyl-4-(4-hydroxyphenoxy)-3-butanone | HCID 19743536 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyano-2-methyl-4-[4-(6-trifluoromethyl-2-quinoxalinyloxy)-phenoxy]-3-butanone | HCID 19743572 | 47.1% |
Reaction Steps
2.20 Grams of a potassium salt of 2-cyano-2-methyl-4-(4-hydroxyphenoxy)-3-butanone and 1.69 g of 2-chloro-6-trifluoromethylquinoxaline were refluxed in 50 nl of N,N-dimethylformamide under heat at 100° C. for 4 hours. The reaction mixture was added to water, and after the mixture was subjected to extraction with chloroform, the extract was concentrated. The residue was separated and purified by column chromatography to give 1.67 g of a compound No. 166 which was a light yellow solid (melting point 113°-115° C.). The yield was 47.1%. The compound No. 166 was analyzed, and the results are shown in Tables 1 to 23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234894 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-a0abf9d09d774dc9b3ac5b3caf56deca |
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| Source note | uspto-grants-1993_08 |
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