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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374704Generated: October 30, 2026

Hydrochloric Acid → HCID 11484643, compound

https://huagongshe.com/reaction/2374704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant2-Acetoxybenzoyl chlorideHCID 79668—
Reactant4-(2-Aminobenzamido)butanoic acidHCID 13442375—
SolventDichloromethaneHCID 6344—
ProductHCID 11484643HCID 11484643—

Reaction Steps

To a suspension of 20.36 g (91.71 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 200 ml of dry methylene chloride, add 42.33 g (391.92 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 11.87 g (117.57 mmol) of triethylamine and a solution of 15.52 g (78.38 mmol) of acetylsalicyloyl chloride dissolved in 20 ml of dry methylene chloride. 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 200 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 (EtOH/H2O). This yields 21.66 g (81%) of 4-[2-(2-hydroxy-benzoylamino)benzoylamino]butanoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462735B2
Source datasetuspto-grants-2008_12
ORD IDord-18e92d89290d4896bd4540fb47774074
Source noteuspto-grants-2008_12