Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970264Erstellt: 24. Oktober 2026

Perfluorobutanesulfonic acid → Diphenyliodanium nonafluorobutane-1-sulfonate

https://huagongshe.com/de/reaction/970264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPerfluorobutanesulfonic acidHCID 67815—
EduktIodonium, diphenyl-, bromide (1:1)HCID 73871—
KatalysatorSilver(II) oxideHCID 92152—
LösungsmittelMethanolHCID 887—
ProduktDiphenyliodanium nonafluorobutane-1-sulfonateHCID 1621693479,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07312014B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-6c2008237a64455bb97166bc766e048d
Quellennotizuspto-grants-2007_12