Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 565743 | HCID 565743 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19022261 | HCID 19022261 | 61.1% |
Reaction Steps
A solution of 20 g (0.085 mol) of hexafluoro-2-(2-furyl)-2-propanol and 8.65 g (0.085 mol) of triethylamine in 25 ml of dry diethyl ether was added dropwise with stirring at a temperature of 20° C. to a solution of 9.8 g (0.09 mol) of α-fluoroacryloyl chloride (obtained according to Example 4) in 25 ml of dry diethyl ether in the course of 30 minutes. The reaction mixture was then stirred at a temperature of 20° C. for a further 4 hours. The resulting solid was filtered off. The filtrate was distilled under reduced pressure after addition of 0.005 g of hydroquinone monomethyl ether. 15.9 g (61 percent of theory) of hexafluoro-2-(2-furyl)-2-propyl α-fluoroacrylate having a boiling point of 55° to 57° C. (under 8 mbar) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05319131 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-b1627498f5f947e692960f55b18db37f |
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| Source note | uspto-grants-1994_06 |
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