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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Methylimidazole | HCID 1390 | — |
| 반응물 | 2-Bromo-1-(3-ethoxyphenyl)ethanone | HCID 22641006 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-methyl-3-[2-(3-ethoxyphenyl)-2-oxoethyl]-1H-imidazolium bromide | HCID 70387602 | 7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04609670 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-3be6da24d2b947c191cab295cfaea4a0 |
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| 출처 메모 | uspto-grants-1986_09 |
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