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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741708Generated: October 30, 2026

Methyl iodide → N-(1-methylimidazol-2-yl)benzylideneamine

https://huagongshe.com/reaction/741708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-[(1E)-phenylmethylidene]-1H-imidazol-2-amineHCID 53795682—
SolventDimethylformamideHCID 6228—
ProductN-(1-methylimidazol-2-yl)benzylideneamineHCID 5384395249.9%

Reaction Steps

N-(2-imidazolyl)benzylideneamine (0.2 g) was dissolved in DMF (4 ml), and potassium t-butoxide (0.15 g) and methyl iodide (0.18 g) were added. The mixture was stirred at room temperature for 3 hours. The solvent was evaporated, and water was added. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (eluent: chloroform). The resulting crude crystals were recrystallized from diethyl ether--hexane to give the title compound (0.1 g, 49.9%) as pale yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552427
Source datasetuspto-grants-1996_09
ORD IDord-4e1abe74d4f54f24aa0ee8eaf6f59d0b
Source noteuspto-grants-1996_09