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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361459Generated: October 30, 2026

Ethyl 2-methylacetoacetate → HCID 178432194, compound

https://huagongshe.com/reaction/1361459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-Amino-2,4'-dichlorobenzophenoneHCID 3016510—
ReactantHCID 178432175HCID 178432175—
SolventO-XyleneHCID 7237—
ProductHCID 178432194HCID 17843219477%

Reaction Steps

A solution of 2.7 g of 3-chloro-4-(4-chlorobenzoyl)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 31 hr. This reaction solution was cooled, and the precipitated crystals were collected by filtration and were washed with n-hexane to give 2.68 g of a mixture of 5-chloro-6-(4-chlorobenzoyl)-4-hydroxy-2,3-dimethyl-quinoline with 7-chloro-6-(4-chlorobenzoyl)-4-hydroxy-2,3-dimethyl-quinoline (yield 77%). The crystals of the mixture thus obtained were stirred in 40 mL of acetic anhydride with heating at 120 to 125° C. for one hr. The reaction solution was concentrated, and the crude product was then purified by column chromatography on silica gel (BW300, manufactured by Fuji Sylysia Chemical Ltd., solvent: n-hexane/ethyl acetate) to give 1.0 g of 4-acetoxy-5-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (yield 32.6%) and 0.47 g of 4-acetoxy-7-chloro-6-(4-chlorobenzoyl)-2,3-dimethyl-quinoline (yield 15.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880006B2
Source datasetuspto-grants-2011_02
ORD IDord-45ff7f3812634f8f814fa60441d29692
Source noteuspto-grants-2011_02