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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743930Generated: October 30, 2026

Bromobenzene → Triphenylsulfonium Tetrafluoroborate

https://huagongshe.com/reaction/743930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantTetrafluoroboric acidHCID 28118—
ReactantMagnesiumHCID 5462224—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductTriphenylsulfonium TetrafluoroborateHCID 2760877—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of magnesium turning (12 g) in ethyl ether (500 ml), bromobenzene (83.5 g, 0.54 mole) was added dropwise under reflux with stirring and continued to stir for 1 hour under reflux. to this Grignard reagent, benzene (500 ml) was added and concentrated until 500 ml. To this resultant mixture, a solution of diphenylsulfoxide (30 g, 0.15 mole) in benzene (200 ml) was added and reacted with stirring for 40 hours under reflux. After the reaction mixture was cooled to 0° C., 40% tetrafluoroboric acid (50 ml) was added dropwise at 0°-5° C. and reacted with stirring for 5 hours at the same temperature. After standing at room temperature overnight, the aqueous layer separated was extracted with methylene chloride (100 ml×3), the organic layer was washed with H2O, dried over anhydrous sodium sulfate and dried. The residual crude solid was recrystallized from chloroform/ethyl ether to give 28 g of triphenylsulfonium tetrafluoroborate as white crystals. m.p. 291°-292° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05558971
Source datasetuspto-grants-1996_09
ORD IDord-f9f2568c290d4541813e1510b6645103
Source noteuspto-grants-1996_09