Tetrafluoroboric acid → Diphenyliodonium Tetrafluoroborate
反応式
S(=O)(=O)(O)[O-].[C:6]1([I+:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[F:19][B-:20]([F:23])([F:22])[F:21].[H+].P(O)(O)O.[Cl-].C1([I+]C2C=CC=CC=2)C=CC=CC=1>O.F[B-](F)(F)F.[Ag+]>[F:19][B-:20]([F:23])([F:22])[F:21].[C:13]1([I+:12][C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1参加物
実験手順
The aromatic iodonium complex salts may be prepared by metathesis of corresponding aromatic iodonium simple salts (such as, for example, the diphenyliodonium bisulfate) in accordance with the teachings of Beringer, et al., J. Am. Chem. Soc 81,342 (1959). Thus, for examples, the complex salt diphenyliodonium tetrafluoroborate is prepared by the addition at 60° C. of an aqueous solution containing 29.2 g (150 millimoles) silver fluoroborate, 2 g. fluoroboric acid, and 0.5 g phosphorous acid in about 30 ml of water to a solution of 44 g (139 millimoles) of diphenyliodonium chloride. The silver halide that precipitates is filtered off and the filtrate concentrated to yield diphenyliodonium fluoroborate which may be purified by recrystallization.
後処理
- customis prepared by the addition at 60° C. of an aqueous solution
- customThe silver halide that precipitates
- filtrationis filtered off
- concentrationthe filtrate concentrated
出典と根拠
- ORDレコード
- ord-44f9ce577dfd4dff9a2a2ba86cf430a4
- 出典データセット
- uspto-grants-1999_01
- 特許番号
- US05856373
反応ノート
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