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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432534Generated: October 25, 2026

Diethyl Ether → Di(1-naphthyl)phenylsulfonium triflate

https://huagongshe.com/reaction/432534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDi(1-naphthyl)sulfideHCID 625448—
ReactantDiphenyliodonium trifluoromethanesulfonateHCID 2737137—
CatalystCupric benzoateHCID 164650—
SolventWaterHCID 962—
ProductDi(1-naphthyl)phenylsulfonium triflateHCID 2264440290%

Reaction Steps

Di(1-naphthyl)sulfide (3 g, 0.0104 mole), diphenyliodonium triflate (5.8 g, 0.0135 mole) and copper benzoate (0.08 g, 0.003 mole) are heated without solvent for 3 hours at 120-145° C. under a nitrogen atmosphere. After cooling down, 75 ml ether was added and the mixture vigorously stirred overnight to achive solidification. Filtration and washing with ether yielded a brown solid, which was dissolved in hot water, the solution filtered and the water removed in vacuo. The resulting white solid was stirred in 50 ml ethyl ether for 24 hours, the mixture filtered and the residue washed with ethyl ether, yielding 4.8 g (90%) of the title compound, di-(1-naphthyl)phenylsulfonium triflate. The structure was confirmed by 1H/13C NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664022B1
Source datasetuspto-grants-2003_12
ORD IDord-7272e59530114867b82c8afcbf50b0ba
Source noteuspto-grants-2003_12