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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386423Generated: November 1, 2026

Imidazole → 2-(1H-imidazol-1-yl)-1-phenylethanol

https://huagongshe.com/reaction/1386423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantStyrene OxideHCID 7276—
CatalystPyridineHCID 1049—
SolventEthanolHCID 702—
Product2-(1H-imidazol-1-yl)-1-phenylethanolHCID 3223935.2%

Reaction Steps

A solution of 17.6 g (0.258 mole 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 tip 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265422B1
Source datasetuspto-grants-2001_07
ORD IDord-a99236898a674c1ca5208e9fd551c5ea
Source noteuspto-grants-2001_07