HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64608Generated: October 28, 2026
Dimethyl Sulfoxide → Dimethyl sulfide ditriflate
https://huagongshe.com/reaction/64608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl sulfide ditriflate | HCID 13658025 | — |
Reaction Steps
In carrying out the first step of the conversion the selected amino pyrazine of formula III, the reagent is prepared by mixing dimethylsulfoxide in methylene chloride and cooled to -78° C. To the cooled solution is added trifluoromethane sulfonic anhydride in a ratio of approximately 3 moles dimethylsulfoxide to 2 moles of anhydride to produce dimethyl sulfide ditriflate of the formula ##STR8## Then, there is added to the cooled solution of VI the selected amino pyrazine of formula III while maintaining the temperature of the reaction mixture at -78° C. to produce the sulfilimine of formula IV. The resulting suspension is made alkaline with aqueous sodium bicarbonate or sodium hydroxide. Additional methylene chloride is added and the product extracted into the methylene chloride phase which is separated and evaporated to remove the volatile organic solvent leaving the sulfilimine IV as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04609659 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-d5fee6eb66ee44f491ac168076542c6e |
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| Source note | uspto-grants-1986_09 |
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