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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-chlorobenzoate | HCID 81785 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-Amino-3-(2-quinolon-3-yl)propionic acid | HCID 13342097 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid | HCID 13342103 | 9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE034722 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-e1a9a765c6874c579b1f5c43c8b29d08 |
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| Source note | uspto-grants-1994_09 |
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