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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490048Generated: October 25, 2026

Triphenylsulfonium chloride → Triphenylsulfonium 1,1,3,3,3-pentafluoro-2-benzoyloxypropane-1-sulfonate

https://huagongshe.com/reaction/490048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantSodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropanesulfonateHCID 58112889—
SolventDichloromethaneHCID 6344—
ProductTriphenylsulfonium 1,1,3,3,3-pentafluoro-2-benzoyloxypropane-1-sulfonateHCID 2311849075%

Reaction Steps

To 50 g of dichloromethane were added an amount (corresponding to 0.011 mole) of the triphenylsulfonium chloride aqueous solution of Synthesis Example 1 and 3.6 g (0.01 mole) of sodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate synthesized in Synthesis Example 9, followed by stirring. The organic layer was separated and washed with 50 g of water three times. The organic layer was concentrated and 25 g of diethyl ether was added to the residue for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 4.5 g (yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07527912B2
Source datasetuspto-grants-2009_05
ORD IDord-437fe514f98e4a9389846a977ea3d6b7
Source noteuspto-grants-2009_05