Trifluoromethanesulfonic acid → Ethylpiperidinium Trifluoromethanesulfonate
反応式
[CH2:1]([NH+:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH3:2].[F:9][C:10]([F:16])([F:15])[S:11]([OH:14])(=[O:13])=[O:12]>>[F:9][C:10]([F:16])([F:15])[S:11]([O-:14])(=[O:13])=[O:12].[CH2:1]([NH+:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH3:2]参加物
3
実験手順
Equimolar amounts of ethylpiperidinium and trifluoromethanesulfonic acid were weighed in a glove box under argon atmosphere. The weighed ethylpiperidinium and trifluoromethanesulfonic acid were mixed and stirred while being cooled by liquid nitrogen, thus obtaining a target ionic conductor.
後処理
- temperaturewhile being cooled by liquid nitrogen
- customthus obtaining a target ionic conductor
出典と根拠
- ORDレコード
- ord-85528ab2c6dd45e5a5e1a95ecacf1a20
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08535849B2
反応ノート
読み込み中…