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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635787Generated: October 26, 2026

Tetramethylammonium pentafluorobenzenesulfonate → Di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate

https://huagongshe.com/reaction/1635787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethylammonium pentafluorobenzenesulfonateHCID 21964803—
Reactant4-t-Amylphenyliodonium sulfateHCID 86585208—
SolventWaterHCID 962—
ProductDi(4-t-amylphenyl)iodonium pentafluorobenzenesulfonateHCID 22486725—

Reaction Steps

t-Amylbenzene (60 g), 39.5 g of potassium iodate, 81 g of acetic anhydride and 170 ml of dichloromethane were mixed, and 66.8 g of concentrated sulfuric acid was slowly added dropwise thereto under ice cooling. After stirring for 2 hours under ice cooling, the mixture was stirred at room temperature for 10 hours. Then, 500 ml of water was added to the reaction solution under ice cooling, and the resulting solution was extracted with dichloromethane. The organic phase was washed with sodium hydrogen carbonate and water, and then concentrated to obtain di (4-t-amylphenyliodonium sulfate. To a solution of tetramethylammonium pentafluorobenzenesulfonate in excess the obtained sulfate was added. Then, 500 ml of water was added to the solution, and 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 obtain di(4-t-amylphenyl)iodonium penta-fluorobenzenesulfonate (III-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511783B1
Source datasetuspto-grants-2003_01
ORD IDord-cd2ce376a95d45cbb3d294d991b8eca5
Source noteuspto-grants-2003_01