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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071964Generated: November 4, 2026

Hydrochloric Acid → [4-(4,5-Dihydro-1H-imidazol-2-yl)phenyl]acetic acid

https://huagongshe.com/reaction/1071964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylenediamineHCID 3301—
ReactantSodium HydroxideHCID 14798—
Reactant4-Cyanophenylacetic acidHCID 79587—
SolventEthanolHCID 702—
Product[4-(4,5-Dihydro-1H-imidazol-2-yl)phenyl]acetic acidHCID 22390702—

Reaction Steps

To a solution of (4-cyanophenyl)acetic acid (131 mg, 0.816 mmol) in EtOH (0.5 mL) at 0° C. was bubbled HCl(g) until saturation. Reaction mixture was allowed to warm to room temperature slowly. After overnight stirring, the crude reaction mixture was concentrated in vacuo. This residue was taken up in EtOH (4 mL) and ethylene diamine (0.1 mL, 1.49 mmol) was added. After stirring at room temperature for two hours, the crude reaction mixture was concentrated under reduced pressure and then re-dissolved in DMF (2 mL). To this solution was added 1M NaOH (2 mL, 2 mmol) and the reaction stirred at room temperature for three hours. Crude reaction mixture was neutralized with 1M HCl to a pH 6 and extracted with CHCl3 (4×15 mL). Product was found in the water layer, so combined all layers and concentrated in vacuo, re-dissolved in CHCl3/MeOH, and filtered to remove precipitate. Concentration of the filtrate gives [4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]acetic acid, which was used without further purification. LCMS (ES) 205.1 m/z (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908921B2
Source datasetuspto-grants-2005_06
ORD IDord-5aa0976e8bc44598a08a3afa6f67dd11
Source noteuspto-grants-2005_06