HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635786Generated: October 30, 2026
Sulfuric Acid → 4-t-Amylphenyliodonium sulfate
https://huagongshe.com/reaction/1635786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | tert-Amylbenzene | HCID 16295 | — |
| Reactant | Potassium Iodate | HCID 23665710 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-t-Amylphenyliodonium sulfate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06511783B1 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-4064cd6803d84205a836c83ab266dd35 |
|---|
| Source note | uspto-grants-2003_01 |
|---|