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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726914Generated: October 25, 2026

Chlorobenzene → Bis(4-chlorophenyl)iodonium trifluoromethanesulfonate

https://huagongshe.com/reaction/726914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 19708102HCID 19708102—
ReactantPotassium IodateHCID 23665710—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventAcetic AnhydrideHCID 7918—
ProductBis(4-chlorophenyl)iodonium trifluoromethanesulfonateHCID 223897978.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 20.0 grams (178 mmol, 1 eq) of chlorobenzene in 30 mL of acetic anhydride and 19.0 grams (88.8 mmol, 0.5 eq) of potassium iodate cooled to 0° C. was added 26.7 grams (15.7 mL, 178 mmol, 1.0 eq) of triflic acid at such a rate that the reaction temperature did not exceed 0° C. The mixture was allowed to warm to room temperature slowly and stirred for 14 hours. Approximately 45 mL of water was added to the reaction mixture at 0°-20° C. followed by methylene chloride. The precipitate dissolved in the methylene chloride and the organic phase was washed with water, aqueous sodium bicarbonate, and water, and concentrated in vacuo. This material was recrystallized from a mixture of 20 mL of isopropanol and 35 mL of hexane to give 7.62 grams (8.6% yield). A second crop was obtained from the mother liquor, 2.5 grams (total yield 11.4%). The product contains less than 7% of the isomeric 2-chlorophenyl-4-chlorophenyliodonium triflate and a small amount of uncharacterized impurity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710320
Source datasetuspto-grants-1998_01
ORD IDord-bb5b5e5a7c8b45098523c14273ff6ddc
Source noteuspto-grants-1998_01