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) within 25 min obtaining a colorless precipitate. 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%) pyridinium tetrafluoroborate as colorless crystals.
後処理
- customobtaining a colorless precipitate
- 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-79801c72926e4e53b33ff500a6e9e9fd
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08754111B2
関連ノート
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