HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368353Generated: October 31, 2026
Imidazole → 2-(1H-imidazol-1-yl)-1-phenylethanol
https://huagongshe.com/reaction/368353
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Styrene Oxide | HCID 7276 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(1H-imidazol-1-yl)-1-phenylethanol | HCID 32239 | 35.2% |
Reaction Steps
A solution of 17.6 g (0.258 mol) of imidazole in 100 mL of absolute EtOH was treated with 0.6 mL (4.0 mmol) of pyridine and refluxed for 25 minutes. This was then treated dropwise with a solution of 31.06 g (0.258 mol) of styrene oxide and the solution heated at reflux overnight. The solvent was removed under reduced pressure and the residue taken up in Et2O and washed with H2O. A solid separated which was collected and dissolved in warm CHCl3 /EtOAc. The organic phase was washed with saturated NaCl and dried over MgSO4. Treatment of the filtrate with charcoal, filtering, and concentrating to 1/3 volume caused a solid to separate. There was collected 17.09 g (35% yield) of the product as a white solid, mp 146-148° C. The structure was confirmed by NMR and mass spectroscopy. MS m/z 189 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133303 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-8336d8604b2f40ef9996e218375cc372 |
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| Source note | uspto-grants-2000_10 |
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