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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584039Generated: October 25, 2026

Heptafluorobutyric acid → Triphenylsulfonium heptafluorobutanoate

https://huagongshe.com/reaction/584039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptafluorobutyric acidHCID 9777—
ReactantSulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 11729320—
CatalystTetramethylammonium chlorideHCID 6379—
SolventMethanolHCID 887—
ProductTriphenylsulfonium heptafluorobutanoateHCID 22328343119.2%

Reaction Steps

In aqueous methanol solution were dissolved 20.6 g (50 mmol) of the resulting triphenylsulfonium trifluoromethanesulfonate, and passed through an activated strong base type anion exchange resin (Amberlite IRA-900 by Organo Corp.). To the elutant solution was added 24.8 g (60 mmol) of heptafluorobutyric acid and allowed reacting with stirring at room temperature for 1 hour. After completion of the reaction, the solvent was removed and the residue was dissolved in 200 ml methylene chloride, washed with water 3 times and concentrated under reduced pressure to give 28.4 g (yield: 84%) of triphenylsulfonium heptafluorobutanoate as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924323B2
Source datasetuspto-grants-2005_08
ORD IDord-6837c286a7ce4d37b3d50fd655588b40
Source noteuspto-grants-2005_08