HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → Bis(4-tert-butylphenyl)iodonium p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Iodonium, bis[4-(1,1-dimethylethyl)phenyl]-, acetate | HCID 21909498 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Bis(4-tert-butylphenyl)iodonium p-toluenesulfonate | HCID 16216932 | 92.3% |
Reaction Steps
Bis(p-tert-butylphenyl)iodonium acetate (467 mg; 1.0 mmol) and methyl p-toluenesulfonate (204 mg; 1.1 mmol) were suspended in t-butyl methyl ether (5 ml). The suspension was heated at 55° C.-58° C. and refluxed for 5 hours while being stirred. The reaction mixture was cooled, and formed white solid was removed through filtration. The white solid was washed with t-butyl methyl ether, and dried under vacuum, to thereby yield 521 mg of bis(p-tert-butylphenyl)iodonium p-toluenesulfonate (yield: 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335787B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-bab00b99c87a4235bfe1c65b95a4d765 |
| Source note | uspto-grants-2008_02 |