HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374507Generated: November 1, 2026
Tetrafluoroboric acid → Diphenyliodonium Tetrafluoroborate
https://huagongshe.com/reaction/1374507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Diphenyliodonium chloride | HCID 73870 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Reactant | Iodonium, diphenyl-, hexafluorophosphate(1-) (1:1) | HCID 2737136 | — |
| Catalyst | Silver tetrafluoroborate | HCID 159722 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diphenyliodonium Tetrafluoroborate | HCID 11122160 | — |
Reaction Steps
The aromatic iodonium complex salts such as diphenyliodonium hexafluorophosphate may be prepared by metathesis of corresponding aromatic iodonium simple salts (such as, for example, diphenyliodonium bisulfate) in accordance with the teachings of Beringer et al., J. Am. Chem. Soc., 81, 342 (1959). Thus, for example, the complex salt diphenyliodonium tetrafluoroborate was prepared by the addition at 60° C. of an aqueous solution containing 29.2 grams (g) silver fluoroborate, 2 g fluoroboric acid, and 0.5 g phosphorous acid in about 30 milliliters (mL) of water to a solution of 44 g (139 millimoles) of diphenyliodonium chloride. The silver halide that precipitated was filtered off and the filtrate concentrated to yield diphenyliodonium fluoroborate, which may be purified by recrystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166409B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-326d390332b54d6abe7cfff885ba1343 |
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| Source note | uspto-grants-2007_01 |
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