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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361452Generated: October 30, 2026

Ethyl 2-methylacetoacetate → HCID 178432191, compound

https://huagongshe.com/reaction/1361452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-(4-Trifluoromethoxyphenoxy)-3-trifluoromethylanilineHCID 86094867—
SolventO-XyleneHCID 7237—
ProductHCID 178432191HCID 17843219141.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880006B2
Source datasetuspto-grants-2011_02
ORD IDord-6ab3d22c39704a6c87f18edf495c3fe5
Source noteuspto-grants-2011_02