1-Ethyl-1H-imidazole → N-ethylimidazole bis(trifluoromethylsulfonyl)imide
反応式
[N-:1]([S:9]([C:12]([F:15])([F:14])[F:13])(=[O:11])=[O:10])[S:2]([C:5]([F:8])([F:7])[F:6])(=[O:4])=[O:3].[CH2:16]([N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1)[CH3:17]>>[N-:1]([S:2]([C:5]([F:8])([F:6])[F:7])(=[O:4])=[O:3])[S:9]([C:12]([F:15])([F:14])[F:13])(=[O:11])=[O:10].[CH2:16]([N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1)[CH3:17]参加物
3
実験手順
To 1.0 g of bis(trifluoromethylsulfonyl)imide was added dropwise 0.34 g of N-ethylimidazole in a nitrogen atmosphere in a glove box, and the solution was stirred overnight to obtain N-ethylimidazole bis(trifluoromethylsulfonyl)imide (EtIm+TFSI−) as a colorless transparent liquid. The resulting salt had a melting point of 6.6° C.
出典と根拠
- ORDレコード
- ord-6f3418108ae64076a6578f9a7953d94e
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07563850B2
反応ノート
読み込み中…