Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Perfluoromethoxypropionyl fluoride | HCID 120237 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 22987397 | HCID 22987397 | 130.9% |
Reaction Steps
Into a clean dry 600 mL Parr reactor were added 11.6 g (0.20 mol) of anhydrous potassium fluoride and 113.5 g of anhydrous diglyme. The contents of the reactor were stirred and cooled with dry ice, then 230 g (0.96 mol) of CF3OCF2CF2COF (approximately 97 percent purity) was added to the sealed reactor using isolated vacuum. With the reactor at 80° C. and pressure of 80 psig (4900 torr), 154 g (1.03 mol) of CF2═CFCF3 was gradually added over a 3½ hour time period. Following a one hour reaction hold time, the product was recovered from the reaction mixture by distillation and phase split prior to fractionation to give 100 g of 1,1,2,2,4,5,5,5-octafluoro-1-trifluoromethoxy-4-trifluoromethylpentan-3-one, having a boiling point of 77° C. and a purity of 99.8% as determined by gas chromatography. The structure was confirmed by gas chromatography and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06478979B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-b861a45b807b4575b99db3800ba085c5 |
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| Source note | uspto-grants-2002_11 |
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