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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374705Generated: October 30, 2026

Hydrochloric Acid → HCID 23118552, compound

https://huagongshe.com/reaction/2374705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant2-Acetoxybenzoyl chlorideHCID 79668—
ReactantHCID 23118560HCID 23118560—
SolventDichloromethaneHCID 6344—
ProductHCID 23118552HCID 23118552—

Reaction Steps

To a suspension of 1.61 g (6.81 mmol) of 5-(2-aminobenzoylamino)pentanoic acid in 20 ml of dry methylene chloride, add 1.41 g (11.94 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 0.88 g (8.73 mmol) of triethylamine and a solution of 1.15 g (5.82 mmol) of 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 20 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 1.26 g (61%) of 5-[2-(2-hydroxybenzoylamino) benzoyl-amino]pentanoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462735B2
Source datasetuspto-grants-2008_12
ORD IDord-99ae35efa4b74c528577ddbfa9c83e73
Source noteuspto-grants-2008_12