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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767431Generated: November 2, 2026

Tetramethylene sulfoxide → HCID 87825836, compound

https://huagongshe.com/reaction/1767431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethylene sulfoxideHCID 1128—
ReactantNaphthalene, 2-butoxy-HCID 82664—
ReactantPotassium perfluorobutanesulfonateHCID 23675274—
ReactantPhosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 87825836HCID 8782583694%

Reaction Steps

Next, 2.9 g (0.05 mol) of tetramethylene sulfoxide was added to 5.0 g (0.025 mol) of the 2-n-butoxynaphthalene and 15 g of Eaton's reagent (Aldrich), followed by 24 hours of stirring at room temperature. 200 g of water and 50 g of diethyl ether were added to the reaction mixture for separation into two layers. To the aqueous layer, 8.5 g (0.025 mol) of potassium perfluorobutanesulfonate and 100 g of dichloromethane were added, followed by one hour of stirring at room temperature. The organic layer separated was washed three times with 50 g of water, after which the solvent was evaporated off on a rotary evaporator. The oily matter was recrystallized from ethyl acetate, filtered and dried. There was obtained 13.8 g of the end compound, 2-n-butoxy-1-naphthyltetrahydrothiophenium perfluorobutanesulfonate (yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235343B2
Source datasetuspto-grants-2007_06
ORD IDord-3e70d6adfeba43a3b449cac32285533e
Source noteuspto-grants-2007_06