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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethylammonium pentafluorobenzenesulfonateHCID 21964803—
Reactant4-t-Amylphenyliodonium sulfateHCID 86585208—
SolventWaterHCID 962—
ProductDi(4-t-amylphenyl)iodonium pentafluorobenzenesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887645B2
Source datasetuspto-grants-2005_05
ORD IDord-806f0db4e285436185823604d705889d
Source noteuspto-grants-2005_05