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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374715Generated: October 26, 2026

Hydrochloric Acid → 4-[2-(4-Nitrobenzoylamino)benzoylamino]butanoic acid

https://huagongshe.com/reaction/2374715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-Aminobenzamido)butanoic acidHCID 13442375—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-[2-(4-Nitrobenzoylamino)benzoylamino]butanoic acidHCID 23118562—

Reaction Steps

To a suspension of 2.14 g (9.63 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 40 ml of dry methylene chloride, add 1.83 g (16.87 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 1.24 g (12.33 mmol) of triethylamine and a suspension of 1.53 g (8.22 mmol) of 4-nitrobenzoyl chloride in 10 ml of dry ethyl acetate. Allow the reaction to stir for 30 minutes in an ice bath and 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 oil has completely disappeared. Immediately acidify with concentrated HCl, filter the resulting solid and wash several times with water and with ether. Purify the reaction product by recrystallization in dioxane/H2O . This yields 1.33 g (43%) of 4-[2-(4-nitrobenzoylamino) benzoylamino] butanoic acid as a cream-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462735B2
Source datasetuspto-grants-2008_12
ORD IDord-8814dd0661c14bf197e4fabd3bd46628
Source noteuspto-grants-2008_12