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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374709Generated: October 30, 2026

Chloride → HCID 23118569, compound

https://huagongshe.com/reaction/2374709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13442366HCID 13442366—
SolventDichloromethaneHCID 6344—
ProductHCID 23118569HCID 23118569—

Reaction Steps

To a suspension of 0.5 g (2.40 mmol) of 3-(2-aminobenzoylamino)propanoic acid in 10 mL of dry methylene chloride, add 0.45 g (4.20 mmol) of trimethylsilyl chloride and allow the reaction to reflux under argon during 2 hours. Then place the flask in an ice bath and add 0.31 g (3.07 mmol) of triethylamine and a solution of 0.40 g (2.05 mmol) of 2-acetylsalicycoyl chloride dissolved in 5 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 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 ether. Purify the reaction product by recrystallization (EtOH/H2O). This yields 0.37 g (56%) of 3-[2-(2-hydroxybenzoylamino)benzoylamino]propanoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462735B2
Source datasetuspto-grants-2008_12
ORD IDord-c8c35331ab49497cb462d161c3c2af69
Source noteuspto-grants-2008_12