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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248694Generated: October 26, 2026

Hydrochloric Acid → Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-

https://huagongshe.com/reaction/248694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantTriethylamineHCID 8471—
Reactant2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductBenzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-HCID 1021555241.3%

Reaction Steps

3-Aminobenzoic acid (1.4 g) is suspended in chloroform (50 ml), and thereto is added triethylamine (2.06 g), and to the mixture is added 2-acetylthiomethyl-3-phenylpropionyl chloride (2.61 g) with stirring under ice cooling, and the mixture is stirred for 30 minutes and further at room temperature three nights. To the reaction mixture is added water, and the mixture is acidified with hydrochloric acid and extracted with chloroform. The extract is washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue is purified by a medium pressure column chromatography with CHP-20P (eluant, water-acetonitrile). The fractions containing the desired compound are collected and concentrated under reduced pressure. The precipitates are separated by filtration and recrystallized from 50% aqueous ethanol to give the title compound (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210266
Source datasetuspto-grants-1993_05
ORD IDord-9086da73e5914ea48feda8ed24d0bab9
Source noteuspto-grants-1993_05