HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674468Generated: October 31, 2026
Dichloromethane → 4-(N,N-diethylaminocarboxy)phenyldiphenylsulfonium perfluorobutanesulfonate
https://huagongshe.com/reaction/1674468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22481373 | HCID 22481373 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(N,N-diethylaminocarboxy)phenyldiphenylsulfonium perfluorobutanesulfonate | HCID 86636106 | 152% |
Reaction Steps
Into a flask, 30 g of 4-hydroxyphenyldiphenylsulfonium perfluorobutanesulfonate and 300 g of dichloromethane were added to prepare a solution. In the flask, a nitrogen gas was blown. To the solution, 17.9 g of N,N-diethylcarbamoyl chloride was added and then 10.5 g of triethylamine was added thereto. The resultant mixture was stirred at room temperature for 1 hour. To the obtained reaction mixture, 100 g of ion-exchanged water was added and an organic layer was obtained by separation. The obtained organic layer was washed with 300 mL of distillated water and then dried over anhydrous magnesium sulfate. Magnesium sulfate was removed by filtration and the obtained filtrate was concentrated. The obtained residue was dried under reduced pressure to obtain 26.7 g of 4-(N,N-diethylaminocarboxy)phenyldiphenylsulfonium perfluorobutanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003296B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-15e5337ccb1844e2992a03ad4f8b7810 |
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| Source note | uspto-grants-2011_08 |
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