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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64652생성일: 2026년 10월 25일

1-Methylimidazole → 1-methyl-3-[2-(3-ethoxyphenyl)-2-oxoethyl]-1H-imidazolium bromide

https://huagongshe.com/reaction/64652

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물2-Bromo-1-(3-ethoxyphenyl)ethanoneHCID 22641006—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물1-methyl-3-[2-(3-ethoxyphenyl)-2-oxoethyl]-1H-imidazolium bromideHCID 703876027%

반응 단계

A solution of 2.9 g (0.012 mol) of 1-bromo-2-(3-ethoxyphenyl)-2-oxoethane in 20 ml of acetonitrile was combined with 1.03 g (0.013 mol) of 1-methylimidazole and the resulting mixture was stirred at room temperature for approximately 18 hours. The mixture was diluted with methanol and the volatiles were evaporated under reduced pressure to a volume of approximately 15 ml. This solution was diluted with ethyl acetate and the precipitated brown solid was collected by filtration. The collected solid was washed with ethyl acetate and dissolved in hot acetonitrile. The mixture was purified with charcoal and upon cooling the solid was collected. The solid was recrystallized from acetonitrile/diethyl ether to provide two crops which were combined and recrystallized three times from isopropyl alcohol to afford 0.27 g of 1-methyl-3-[2-(3-ethoxyphenyl)-2-oxoethyl]-1H-imidazolium bromide as pale yellow flakes. (7% yield) mp=137°-138° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609670
출처 데이터셋uspto-grants-1986_09
ORD IDord-3be6da24d2b947c191cab295cfaea4a0
출처 메모uspto-grants-1986_09