反応式
[F:1][B-:2]([F:5])([F:4])[F:3].[H+].[N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[F:1][B-:2]([F:5])([F:4])[F:3].[NH+:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1参加物
3
実験手順
Tetrafluoroboric acid (250 ml, 2.00 mol) was added to cool (0° C.) pyridine (157.7 ml, 1.95 mol) and within 25 min a colorless precipitate was obtained. After the acid was completely added the mixture was further stirred for 30 min at the same temperature. Then the reaction mixture was filtered. The residue was washed twice with cold ethanol and dried 12 h at high vacuum to yield 201.9 g (60%) pyridiniumtetrafluoroborate as colorless crystals.
後処理
- customwithin 25 min a colorless precipitate was obtained
- additionAfter the acid was completely added the mixture
- filtrationThen the reaction mixture was filtered
- washThe residue was washed twice with cold ethanol
- customdried 12 h at high vacuum
出典と根拠
- ORDレコード
- ord-2276f2b332ac44709ebb2e2b240805ef
- 出典データセット
- uspto-grants-2015_07
- 特許番号
- US09085535B2
関連ノート
読み込み中…