HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240806Generated: October 30, 2026
Hydrochloric Acid → 5-ethyl-4-phenyl-1H-imidazole
https://huagongshe.com/reaction/240806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Amino-1-phenylpropan-1-one;hydrochloride | HCID 204630 | — |
| Reactant | Sodium thiocyanate | HCID 516871 | — |
| Product | 5-ethyl-4-phenyl-1H-imidazole | HCID 14297629 | 45% |
Reaction Steps
An aqueous solution (5 mL) of concentrated hydrochloric acid (0.6 mL) and sodium thiocyanate (1.62 g, 20.03 mmol) was added to a solution of 2-aminopropiophenone hydrochloride (2.00 g, 10.02 mmol) in ethanol (20 mL). The obtained mixture was stirred at 70° C. for 1 hour. The solvent was distilled away, and acetic acid (20 mL) was then added to the residue. The obtained mixture was stirred at 100° C. for 3 hours. Thereafter, water was added to the reaction solution, and the precipitated crude crystals were collected by filtration. Raney Ni was added to a solution of the obtained crude crystals in ethanol (40 mL), and the obtained mixture was then stirred at 70° C. for 2 hours. The reaction solution was filtered with celite, and the filtrate was then concentrated. The residue was washed with acetonitrile, so as to obtain the title compound (0.88 g, yield in two steps: 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08648103B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-a4dcb7a32a0245b294193169c4f5a313 |
|---|
| Source note | uspto-grants-2014_02 |
|---|