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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970264Generated: October 25, 2026

Perfluorobutanesulfonic acid → Diphenyliodanium nonafluorobutane-1-sulfonate

https://huagongshe.com/reaction/970264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluorobutanesulfonic acidHCID 67815—
ReactantIodonium, diphenyl-, bromide (1:1)HCID 73871—
CatalystSilver(II) oxideHCID 92152—
SolventMethanolHCID 887—
ProductDiphenyliodanium nonafluorobutane-1-sulfonateHCID 1621693479.3%

Reaction Steps

To 100 ml of methanol, 3.61 g (0.01 mole) of diphenyliodonium bromide and 1.62 g (0.007 mole) of silver oxide were suspended, then the mixture was reacted at room temperature for 2 hours. To the reaction solution, 4.2 g (0.014 mole) of nonafluorobutanesulfonic acid was added drop-wise at room temperature, followed by reacting at the same temperature for 2 hours while stirring. The thus obtained reaction mixture was filtered and concentrated under reduced pressure, followed by purifying 6.4 g of the residue by column chromatography [Wako gel, C-200; eluent of methylene chloride/methanol=9/1 (v/v)], to obtain 4.6 g of diphenyliodonium nonafluorobutanesulfonate as a colorless crystal. The thus obtained crystal was named acid generator B1. The measurement results of melting point and NMR of acid generator B1 are shown bellow.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312014B2
Source datasetuspto-grants-2007_12
ORD IDord-6c2008237a64455bb97166bc766e048d
Source noteuspto-grants-2007_12