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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968427Generated: October 26, 2026

Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/968427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantSodium hydrideHCID 24758—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
SolventTetrahydrofuranHCID 8028—
Product1-Phenethyl-1H-imidazole-4-carbaldehydeHCID 22289872—

Reaction Steps

Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958402B2
Source datasetuspto-grants-2005_10
ORD IDord-e2df1067444d4e47b08f076064e9aa84
Source noteuspto-grants-2005_10