HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767431Generated: November 2, 2026
Tetramethylene sulfoxide → HCID 87825836, compound
https://huagongshe.com/reaction/1767431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetramethylene sulfoxide | HCID 1128 | — |
| Reactant | Naphthalene, 2-butoxy- | HCID 82664 | — |
| Reactant | Potassium perfluorobutanesulfonate | HCID 23675274 | — |
| Reactant | Phosphorus Pentoxide-Methanesulfonic Acid | HCID 86584057 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87825836 | HCID 87825836 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235343B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-3e70d6adfeba43a3b449cac32285533e |
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| Source note | uspto-grants-2007_06 |
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