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HRID 31546생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/31546

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물TriethylamineHCID 8471—
반응물4-Methylbenzoyl ChlorideHCID 13405—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 178418822HCID 178418822—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(1-Allyl-4-phenyl-1H-imidazole-2-yl)(4-methylphenyl)methanoneHCID 5986332430%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425642B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-bf2eefba035149b195bd8b452f9e4bb0
출처 메모uspto-grants-2008_09