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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635786Generated: October 30, 2026

Sulfuric Acid → 4-t-Amylphenyliodonium sulfate

https://huagongshe.com/reaction/1635786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetic AnhydrideHCID 7918—
Reactanttert-AmylbenzeneHCID 16295—
ReactantPotassium IodateHCID 23665710—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-t-Amylphenyliodonium sulfateHCID 86585208—

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-4064cd6803d84205a836c83ab266dd35
Source noteuspto-grants-2003_01