HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249353Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 22023911, compound
https://huagongshe.com/reaction/2249353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 2,6-Dimethylphenol | HCID 11335 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium perfluorobutanesulfonate | HCID 23675274 | — |
| Reactant | Phosphorus Pentoxide-Methanesulfonic Acid | HCID 86584057 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22023911 | HCID 22023911 | — |
Reaction Steps
8 ml of Eaton's Reagent (from Aldrich, 7.7 wt. % of P2O5 in methanesulfonic acid) through an addition funnel to a mixture of 2.44 g (0.02 mol) of 2,6-dimethylphenol and 1.56 g (0.02 mol) of dimethylsulfoxide in a 50-mL 3-necked round bottom flask equipped with a thermometer, N2 inlet and magnetic stirrer. The rate of the addition was adjusted so that the temperature of the mixture did not rise above 60° C. during addition. After the exotherm had subsided, the reaction mixture was stirred at room temperature for 2 hours and then poured into 40 mL of distilled water. The solution was neutralized to pH=7 by adding ammonium hydroxide solution. The resulting solution was stirred at room temperature for half an hour and then filtered through a filter paper to remove the brown oily side products. The filtrate was added dropwise to a solution of 6.76 g (0.02 mol) of potassium perfluorobutanesulfonate (KPFBuS) in 70 mL water while stirring. The mixture was further stirred overnight. The white precipitate was collected by suction filtration and washed with water and ether three times. The crude product was redissolved in 15-20 mL of ethyl acetate. To this solution, 200-300 mg of aluminum oxide (activated, basic) was added. The mixture was rolled on a roller overnight and then filtered through Celite. The filtrate was precipitated into 100 mL ether while stirring. The white precipitate was collected and further washed with ether three times. Final yield: 2.2 g (23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314700B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-e163e71d104641feb1debd0236ce8550 |
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| Source note | uspto-grants-2008_01 |
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