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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496421Generated: October 25, 2026

Imidazole → (1r)-2-Imidazolyl-1-phenylethan-1-ol

https://huagongshe.com/reaction/496421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPyridineHCID 1049—
Reactant(+)-Styrene oxideHCID 114705—
SolventEthanolHCID 702—
Product(1r)-2-Imidazolyl-1-phenylethan-1-olHCID 6973530932%

Reaction Steps

In a manner similar to that of Example 49, step 1, imidazole (2.83 g, 41.6 mmol) is dissolved in absolute ethanol (45 mL). Pyridine (0.11 mL) is added followed by addition of (R)-(+) styrene oxide (5.0 g, 41.6 mol, Aldrich Chemical Co.), followed by heating at reflux for 18 hours. The mixture is evaporated in vacuo to a syrup and suspended between ethyl ether (250 mL) and water (100 mL) to give a solid precipitate. The suspension is filtered and washed with ethyl ether. The solid is recrystallized from hot ethyl acetate and dried in vacuo (2.52 g, 32% yield). MS: APCI: M+1, 189.1 (M: 188.2). NMR spectrum is consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943183B2
Source datasetuspto-grants-2005_09
ORD IDord-150e80cf7b2f4adaa9053a82b1eba305
Source noteuspto-grants-2005_09