HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085004Generated: November 1, 2026
Tetramethylammonium pentafluorobenzenesulfonate → HCID 86759414, compound
https://huagongshe.com/reaction/2085004
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetramethylammonium pentafluorobenzenesulfonate | HCID 21964803 | — |
| Reactant | Bis{bis[4-(2-methylbutan-2-yl)phenyl]iodanium} sulfate | HCID 71350713 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86759414 | HCID 86759414 | — |
Reaction Steps
Under ice-cooling, 25 g of pentafluorobenzenesulfonyl and 66.8 g of concentrated sulfuric acid was gradually dropwise added to the mixture with ice-cooling. The mixture was stirred with ice-cooling for 2 hours and then at room temperature for 10 hours. With ice-cooling, 500 ml of water was added to the reaction solution, followed by extraction with dichloromethane. The organic phase was washed with sodium bicarbonate and water and then concentrated, thereby a di (4-t-amylphenyl) iodonium sulfate was obtained. The sulfate was added to a solution containing an excess amount of tetramethylammonium pentafluorobenzenesulfonate. Water (500 ml) was added to the solution, followed by extraction with dichloromethane. The organic phase was washed with a 5% aqueous solution of tetramethylammonium hydroxide and water, and then concentrated, thereby di (4-amylphenyl) iodonium pentafluorobenzenesulfonate was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06720128B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-cbffeaf887d84aa2b8069ab2cfffd46d |
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| Source note | uspto-grants-2004_04 |
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