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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31546Erstellt: 25. Oktober 2026

Allyl bromide → (1-Allyl-4-phenyl-1H-imidazole-2-yl)(4-methylphenyl)methanone

https://huagongshe.com/reaction/31546

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktTriethylamineHCID 8471—
Edukt4-Methylbenzoyl ChlorideHCID 13405—
EduktPotassium tert-butoxideHCID 23665647—
EduktHCID 178418822HCID 178418822—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt(1-Allyl-4-phenyl-1H-imidazole-2-yl)(4-methylphenyl)methanoneHCID 5986332430%

Reaktionsschritte

Potassium t-butoxide (2.59 g, 23.1 mmol) was dissolved in DMF (100 ml), and thereto was added 4-phenyl-1H-imidazole (3.00 g, 21 mmol) with stirring. The mixture was stirred at room temperature for 30 minutes, and thereto was added allyl bromide (3.50 g, 31.5 mmol). The mixture was stirred at 40° C. for 4 hours. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated saline, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting residue was dissolved in pyridine (24 ml), and thereto were added successively triethylamine (17.9 g, 17.7 mmol) and 4-toluoyl chloride (3.7 g, 16.3 mmol), and the mixture was stirred at 60° C. for 5 hours. To the reaction solution was added water (50 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with water, 1N diluted hydrochloric acid, and saturated saline, and dried over magnesium sulfate. Then, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give the title compound (760 mg, 30%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425642B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-bf2eefba035149b195bd8b452f9e4bb0
Quellennotizuspto-grants-2008_09