HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172033Generated: October 31, 2026
Diphenyl sulfoxide → HCID 23054313, compound
https://huagongshe.com/reaction/1172033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl sulfoxide | HCID 13679 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-Chlorothioxanthone | HCID 618848 | — |
| Reactant | Potassium hexafluorophosphate | HCID 23688904 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23054313 | HCID 23054313 | 7% |
Reaction Steps
To 320 ml of dichloromethane were suspended 20.2 g (0.1 mol) of diphenylsulfoxide and 24.6 g (0.1 mol) of 2-chlorothioxanthene-9-one, and 28.2 g (0.1 mol) of trifluoromethanesulfonic anhydride was added dropwise thereto at −70 to −60° C., followed by gradually warming to room temperature and reacting with stirring for 3 hours. After completion of the reaction, the obtained reaction solution was washed with water (320 ml×5 times) and 18.4 g (0.1 mol) of potassium hexafluorophosphate and 200 ml of water were added to the obtained dichloromethane layer, followed by stirring at room temperature for 2 hours and fractionating the solution. Then, 9.2 g (0.05 mol) of potassium hexafluorophosphate and 100 ml of water were further added to the obtained dichloromethane layer, followed by stirring at room temperature for 2 hours and fractionating the solution. Then the obtained dichloromethane layer was washed with 200 ml of water and concentrated to dryness under reduced pressure. The obtained crude product was purified by column chromatography to obtain 4.0 g of objective substance as pale yellow glassy substance (yield: 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833691B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-afac1c884c444ec491531d0796bb4ed1 |
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| Source note | uspto-grants-2010_11 |
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