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1,2-Dimethylimidazole → 1,2-Dimethyl-3-propylimidazolium iodide

HRID 449242
ノート
印刷プレビュー

反応式

HRID 449242 の反応式
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[C:3]1[CH3:7].[CH2:8]([I:11])[CH2:9][CH3:10]>C1(C)C=CC=CC=1>[I-:11].[CH3:1][N+:2]1[CH:6]=[CH:5][N:4]([CH2:8][CH2:9][CH3:10])[C:3]=1[CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 156171,2-DimethylimidazoleHCID 336431-Iodopropane

生成物 1

HCID 114597861,2-Dimethyl-3-propylimidazolium iodide収率 92%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

1,2-dimethylimidazole (7.2 g, made by Aldrich) and propyl iodide (12.7 g, made by Kanto Chemical) were stirred in toluene at 75° C. for 15 hours. After the end of the reaction, the reaction mixture was cooled to room temperature and the crude crystals formed were recovered. A mixed solvent of toluene and isopropanol was used for recrystallization. The crystals were dried in vacuo to obtain 1,2-dimethyl-3-propylimidazolium iodide (18.3 g).

後処理

  1. customAfter the end of the reaction
  2. customthe crude crystals formed
  3. customwere recovered
  4. customA mixed solvent of toluene and isopropanol was used for recrystallization
  5. customThe crystals were dried in vacuo

出典と根拠

ORDレコード
ord-4ebc76d7580e4d18916bcf4bab2576f9
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08481849B2

反応ノート

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