Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 13980927 | HCID 13980927 | 74.1% |
Reaction Steps
15.3 g (0.092 mol) of hexafluoroacetone were passed with stirring in the course of 30 minutes at a temperature of 25° C. into a suspension of 5.34 g (0.092 mol) of dried potassium fluoride in 25 ml of dry diethylene glycol dimethyl ether, and the potassium fluoride dissolved. After a further 2 hours of stirring, unreacted hexafluoroacetone was distilled off under reduced pressure (water jet pump). 10 g (0.092 mol) of α-fluoroacryloyl chloride were added at a temperature of 25° C. with stirring to the remaining solution in the course of 5 minutes, and a colorless solid precipitated. The reaction mixture was stirred at a temperature of 25° C. for a further 80 minutes, and 0.005 g of hydroquinone monomethyl ether were then added, which has followed by distillation under a pressure of 40 mbar. 17.6 g (74 percent of theory) of perfluoroisopropyl α-fluoroacrylate having a boiling point of 40° C. (under 165 mbar) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198925 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-c14638817d734fd6a885e124a7d88593 |
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| Source note | uspto-grants-1993_03 |
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