HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361452Generated: October 30, 2026
Ethyl 2-methylacetoacetate → HCID 178432191, compound
https://huagongshe.com/reaction/1361452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-(4-Trifluoromethoxyphenoxy)-3-trifluoromethylaniline | HCID 86094867 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178432191 | HCID 178432191 | 41.1% |
Reaction Steps
A solution of 3.4 g of 4-(4-trifluoromethoxyphenoxy)-3-trifluoromethyl-aniline, 2.4 g of ethyl 2-methylacetoacetate, and 0.3 g of p-toluenesulfonic acid dissolved in 100 mL of xylene was heated under reflux for 36 hr. This reaction solution was cooled, and the precipitated crystals were collected by filtration to give 1.73 g of 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-7-trifluoromethyl-quinoline. The filtrate was concentrated under the reduced pressure to give 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline. Acetic anhydride (40 mL) was added to 2,3-dimethyl-4-hydroxy-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline obtained from the filtrate, and the mixture was heated at 120 to 125° C. for one hr. This reaction solution was concentrated under the reduced pressure, ethyl acetate was then added to the concentrate, and the mixture was washed with brine. Thereafter, the solvent was removed under the reduced pressure, and the crude product was purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 0.35 g of 4-acetoxy-2,3-dimethyl-6-(4-trifluoromethoxyphenoxy)-5-trifluoromethyl-quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880006B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-6ab3d22c39704a6c87f18edf495c3fe5 |
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| Source note | uspto-grants-2011_02 |
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