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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506657Generated: November 1, 2026

Acetonitrile → 4-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazole

https://huagongshe.com/reaction/1506657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantN-bromobutanimideHCID 67184—
Reactant(4-Chlorophenyl)-1-methyl-1H-imidazoleHCID 10856331—
Product4-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazoleHCID 25172146—

Reaction Conditions

Temperature0 °C

Reaction Steps

(4-Chlorophenyl)-1-methyl-1H-imidazole (3 g, 15.5 mmol) was dissolved in ACN (150 mL) and cooled to 0° C. NBS (2.76 g, 15.5 mmol) was added in 3 portions over 5 min. The reaction was stirred at 0° C. for 20 min then let warm to ambient temperature. Solvents were removed in vacuo and the residue partitioned between EtOAc and 20% aqueous KH2PO4. The organics were separated, washed with saturated aqueous NaHCO3, and dried with saturated aqueous NaCl. Solvents were removed in vacuo and the residue purified by column chromatography on silica to provide the desired product. MS (m/z) 273.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09220710B2
Source datasetuspto-grants-2015_12
ORD IDord-41c6eccd80504082ae7e6b03564163d4
Source noteuspto-grants-2015_12