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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057135Generated: October 26, 2026

Methyl p-toluenesulfonate → Bis(4-tert-butylphenyl)iodonium p-toluenesulfonate

https://huagongshe.com/reaction/2057135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantIodonium, bis[4-(1,1-dimethylethyl)phenyl]-, acetateHCID 21909498—
Solventtert-Butyl methyl etherHCID 15413—
ProductBis(4-tert-butylphenyl)iodonium p-toluenesulfonateHCID 1621693292.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335787B2
Source datasetuspto-grants-2008_02
ORD IDord-bab00b99c87a4235bfe1c65b95a4d765
Source noteuspto-grants-2008_02