1-Methylimidazole → 1-methyl-3-[2-(3-ethoxyphenyl)-2-oxoethyl]-1H-imidazolium bromide
反応式
[Br:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH3:13])[CH:6]=1)=[O:4].[CH3:14][N:15]1[CH:19]=[CH:18][N:17]=[CH:16]1>C(#N)C.CO>[Br-:1].[CH3:14][NH+:15]1[CH:19]=[CH:18][N:17]([CH2:2][C:3]([C:5]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH3:13])[CH:6]=2)=[O:4])[CH2:16]1参加物
実験手順
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.
後処理
- customthe volatiles were evaporated under reduced pressure to a volume of approximately 15 ml
- additionThis solution was diluted with ethyl acetate
- filtrationthe precipitated brown solid was collected by filtration
- washThe collected solid was washed with ethyl acetate
- dissolutiondissolved in hot acetonitrile
- customThe mixture was purified with charcoal
- temperatureupon cooling the solid
- customwas collected
- customThe solid was recrystallized from acetonitrile/diethyl ether
- customto provide two crops which
- customrecrystallized three times from isopropyl alcohol
出典と根拠
- ORDレコード
- ord-3be6da24d2b947c191cab295cfaea4a0
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04609670
反応ノート
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