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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23551Generated: October 30, 2026

Hydrochloric Acid → 2-{1-[8-(2,4-Dichlorophenyl)-2-methylquinolin-4-yl]-piperidin-4-ylidene}acetic acid

https://huagongshe.com/reaction/23551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant8-(2,4-Dichlorophenyl)-2-methyl-4-(4-ethoxycarbonyl-methylidenepiperidin-1-yl)quinolineHCID 22574431—
Product2-{1-[8-(2,4-Dichlorophenyl)-2-methylquinolin-4-yl]-piperidin-4-ylidene}acetic acidHCID 12134668—

Reaction Steps

In a mixed solvent of 85% potassium hydroxide (1.3 g) and water (1.4 mL)-ethanol (8 mL), 8-(2,4-dichlorophenyl)-2-methyl-4-(4-ethoxycarbonyl-methylidenepiperidin-1-yl)quinoline (2.3 g) was stirred at 80° C. for 1 hour. The reaction mixture was neutralized with 3 M hydrochloric acid under ice-cooling and stirred under ice-cooling for 2 hours and then at room temperature for 30 minutes. The solid precipitated was collected by filtration to obtain a mixture (1.5 g) of 2-{1-[8-(2,4-dichlorophenyl)-2-methylquinolin-4-yl]-piperidin-4-ylidene}acetic acid and 2-{1-[8-(2,4-dichlorophenyl)-2-methylquinolin-4-yl]-1,2,3,6-tetrahydropyridin-4-yl}acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852732B2
Source datasetuspto-grants-2005_02
ORD IDord-c9ea102d16034504b8ea8da42f826b94
Source noteuspto-grants-2005_02