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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Cyanophenylacetic acid | HCID 79587 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [4-(4,5-Dihydro-1H-imidazol-2-yl)phenyl]acetic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06908921B2 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-5aa0976e8bc44598a08a3afa6f67dd11 |
|---|
| Source note | uspto-grants-2005_06 |
|---|