反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[CH:11][N:10]=[CH:9]2)=[CH:4][CH:3]=1.[CH3:13][I:14]>C1COCC1>[I-:14].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N+:8]2[CH:12]=[CH:11][N:10]([CH3:13])[CH:9]=2)=[CH:6][CH:7]=1参加物
4
実験手順
1-(4-Chlorophenyl)imidazole (0.37 g, 2.07 mmol) is dissolved in THF (5 ml) and subsequently admixed with methyl iodide (1.47 g, 10.4 mmol) and allowed to stand for 20 hours. The precipitate formed is subsequently filtered off and washed with ethanol and with petroleum ether and subsequently dried under reduced pressure. This gives 0.46 g of 1-(4-chlorophenyl)-3-methylimidazolium iodide.
後処理
- customThe precipitate formed
- filtrationis subsequently filtered off
- washwashed with ethanol and with petroleum ether
- customsubsequently dried under reduced pressure
出典と根拠
- ORDレコード
- ord-676487415dcd4a69a0c42a1697107604
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877937B2
関連ノート
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