Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23133152 | HCID 23133152 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87490629 | HCID 87490629 | — |
Reaction Steps
Bis[4-hydroxylphenyl]phenysulfonium perfluorobutanesulfonate (10 g) and acetone were placed into a reaction vessel equipped with an agitator, a thermometer, a reflux condenser, and a tube for introducing nitrogen gas into the vessel. Under a nitrogen blanket, 4.6 g of potassium carbonate was added to the reaction vessel and the mixture was stirred for an hour. Acetic anhydride 3.43 gram was added and stirred overnight at room temperature. Dichloromethane (150 ml) and water were added to the reaction vessel and the mixture was stirred for 2 hours. The mixture was then placed into a separatory funnel and the organic (dichloromethane) layer was retained. The dichloromethane layer was washed several times with water, dried over anhydrous sodium sulfate, filtered, and the remaining volatile materials were evaporated to leave an oil. Ether was added to the oil and the mixture was stirred vigorously. A very sticky solid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678528B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-64e7cbdb206146d3b31cf622fbd1a0cb |
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| Source note | uspto-grants-2010_03 |
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