HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179875Generated: October 31, 2026
Tetramethylammonium pentafluorobenzenesulfonate → Di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate
https://huagongshe.com/reaction/2179875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetramethylammonium pentafluorobenzenesulfonate | HCID 21964803 | — |
| Reactant | 4-t-Amylphenyliodonium sulfate | HCID 86585208 | — |
| Solvent | Water | HCID 962 | — |
| Product | Di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate | HCID 22486725 | — |
Reaction Steps
60 g of t-amylbenzene, 39.5 g of potassium iodate, 81 g of acetic anhydride and 170 ml of dichloromethane were mixed together. Then 66.8 g of conc. sulfuric acid was slowly added dropwise thereinto under ice-cooling. After stirring under ice-cooling for 2 hours, the mixture was stirred at room temperature for additional 10 hours. 500 ml of water was added to the liquid reaction mixture under ice-cooling and the mixture was extracted with dichloromethane. The organic phase was washed with sodium hydrogencarbonate and water and then concentrated to give (4-t-amylphenyl)iodonium sulfate. This sulfate was added to a solution of tetramethylammonium pentafluorobenzenesulfonate in excess. After adding 500 ml of water, the solution was extracted with dichloromethane. Then the organic phase was washed with a 5% aqueous solution of tetramethylammonium hydroxide and water and then concentrated to give di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate (III-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06887645B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-806f0db4e285436185823604d705889d |
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| Source note | uspto-grants-2005_05 |
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