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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252626Generated: November 1, 2026

Methyl iodide → 1-methyl-4-phenyl-1H-imidazole

https://huagongshe.com/reaction/252626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418822HCID 178418822—
SolventDichloromethaneHCID 6344—
Product1-methyl-4-phenyl-1H-imidazoleHCID 2748782—
Product1-Methyl-5-phenyl-1H-imidazoleHCID 3746343—

Reaction Steps

To a slurry of sodium hydride, 60% in mineral oil (1.2 g, 31 mmol) in 100 mL anhyd. THF at 0° C. was added 4-phenylimidazole (4.00 g, 28 mmol) in small portions under nitrogen. Upon complete addition, the reaction was homogeneous and orange. After 10 min, methyl iodide (2.1 ml, 33 mmol) was added and the reaction was allowed to warm to ambient temperature. After 2 h, the reaction was quenched with 10 mL water and concentrated in vacuo. The resulting liquid was partitioned between water/brine and DCM. The aqueous layer was extracted with DCM (4×). The combined organic extracts were dried over anhyd sodium sulfate, filtered, and concentrated in vacuo to give an orange solid. This was dissolved in dichloromethane and purified by silica gel chromatography, 120 g, 60 min, 0-50% 90/10 DCM/MeOH in DCM, to give 1-methyl-4-phenyl-1H-imidazole and 1-methyl-5-phenyl-1H-imidazole as off-white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868177B2
Source datasetuspto-grants-2011_01
ORD IDord-63c9de5a516346e4b0c2d93c810b0c16
Source noteuspto-grants-2011_01