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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619150Generated: November 1, 2026

Acetamidine monohydrochloride → 5-(3-bromo-4-methylphenyl)-2-methyl-1H-imidazole

https://huagongshe.com/reaction/1619150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantPotassium BicarbonateHCID 516893—
Reactant2-Bromo-1-(3-bromo-4-methylphenyl)ethanoneHCID 12622499—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(3-bromo-4-methylphenyl)-2-methyl-1H-imidazoleHCID 581704635%

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium bicarbonate (2.10 g, 20.7 mmol) was added portionwise to a solution of acetimidamide hydrochloride (1.06 g, 11.2 mmol) in tetrahydrofuran (20 mL) and water (5 mL). The resulting mixture was heated to reflux and 2-bromo-1-(3-bromo-4-methylphenyl)ethanone (preparation 58a, 2.74 g, 9.4 mmol) was added dropwise over a period of 20 minutes. After 3 hours, further acetamidamide hydrochloride (1.06 g, 11.2 mmol) and potassium bicarbonate (1.03 g, 10.1 mmol) were added and the was mixture refluxed overnight. The mixture was evaporated to dryness and partitioned between 2M aqueous hydrochloric acid and ethyl acetate. The acidic aqueous layer was bascified with solid sodium hydroxide and extracted with ethyl acetate. The organic layer was dried (MgSO4) and the solvent was evaporated under reduced pressure to give a semi solid. This semi solid was heated in vacuo at 70° C. for one hour in order to remove excess acetamidamide to give the pure title compound (0.10 g, 5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772288B2
Source datasetuspto-grants-2014_07
ORD IDord-c2e7c353795a4bc6bf3d8a9af71cdafa
Source noteuspto-grants-2014_07