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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249353Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 22023911, compound

https://huagongshe.com/reaction/2249353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantNitrogenHCID 947—
Reactant2,6-DimethylphenolHCID 11335—
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium perfluorobutanesulfonateHCID 23675274—
ReactantPhosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
SolventWaterHCID 962—
ProductHCID 22023911HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314700B2
Source datasetuspto-grants-2008_01
ORD IDord-e163e71d104641feb1debd0236ce8550
Source noteuspto-grants-2008_01