HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374708Generated: October 27, 2026
Hydrochloric Acid → 4-[2-(2-Nitrobenzoylamino)benzoylamino]butanoic acid
https://huagongshe.com/reaction/2374708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-Aminobenzamido)butanoic acid | HCID 13442375 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[2-(2-Nitrobenzoylamino)benzoylamino]butanoic acid | HCID 23118556 | — |
Reaction Steps
To a suspension of 3.90 g (17.50 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 40 ml of dry ethyl acetate, add 3.26 g (17.56 mmol) of 2-nitrobenzoyl chloride dissolved in 5 ml of dry ethyl acetate and 1.76 g of triethylamine. Allow the reaction mixture to stir for 24 hours at room temperature. Eliminate the solvent at low pressure, add 30 ml of 10% NaOH to the crude product and continue stirring the mixture until the solid has completely disappeared. Immediately acidify with concentrated HCl and extract the product with ethyl acetate. Eliminate the solvent at low pressure and recombine the crude product with dry ether, obtaining a white solid. Purify the reaction product by recrystallization (EtOH/H2O). This yields 3.34 g (51%) of 4-[2-(2-nitrobenzoylamino)benzoylamino]butanoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462735B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-72041cb47dfe415d8cde2bb5502f23da |
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| Source note | uspto-grants-2008_12 |
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