Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225342Generated: October 25, 2026

Ethyl 4-chlorobenzoate → 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid

https://huagongshe.com/reaction/2225342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chlorobenzoateHCID 81785—
ReactantSodium ethoxideHCID 2723922—
Reactant2-Amino-3-(2-quinolon-3-yl)propionic acidHCID 13342097—
SolventEthanolHCID 702—
Product2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acidHCID 133421039%

Reaction Steps

In 100 ml of ethanol, 1.66 g of ethyl p-chlorobenzate, 0.5 g of sodium ethylate and 2.09 g of 2-amino-3-(2-quinolon-3-yl)propionic acid were added and the whole mixture was placed in an autoclave. The reaction was carried out under 110 atmospheric pressure at 140°-150° C. for 6 hours. After completion of the reaction, the reaction mixture was cooled and concentrated under a reduced pressure. The residue was dissolved in 200 ml of chloroform, washed with 1%-potassium carbonate aqueous solution, a diluted hydrochloric acid and water in this order, then the chloroform layer was dried with sodium sulfate. The solvent was removed by distillation, the residue was recrystallized from ethanol-water to obtain 300 mg of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powdery product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE034722
Source datasetuspto-grants-1994_09
ORD IDord-e1a9a765c6874c579b1f5c43c8b29d08
Source noteuspto-grants-1994_09