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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374707Generated: October 27, 2026

Hydrochloric Acid → HCID 23118553, compound

https://huagongshe.com/reaction/2374707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23110866HCID 23110866—
Reactant2-Acetylsalicyloyl chlorideHCID 57361564—
SolventDichloromethaneHCID 6344—
ProductHCID 23118553HCID 23118553—

Reaction Steps

To a suspension of 0.30 g (1.20 mmol) of 6-(2-aminobenzoylamino)hexanoic acid in 5 ml of dry methylene chloride, add 0.23 g (2.10 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 0.15 g (1.53 mmol) of triethylamine and a solution of 0.20 g (2.05 mmol) of 2-acetylsalicyloyl 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 10 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 0.24 g (62%) of 6-[2-(2-hydroxybenzoylamino)benzoylamino]hexanoic as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462735B2
Source datasetuspto-grants-2008_12
ORD IDord-0f69f3099f1848d0a6f9ce4dbb992819
Source noteuspto-grants-2008_12