Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 520085 | HCID 520085 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13980930 | HCID 13980930 | 83.1% |
Reaction Steps
A solution of 40 g (0.153 mol) of 2-(4-fluorophenyl)-hexafluoro-2-propanol and 15.5 g (0.153 mol) of triethylamine in 75 ml of dry diethyl ether were added dropwise with stirring at a temperature of 25° C. to a solution of 18 g (0.166 mol) of α-fluoroacryloyl chloride (obtained according to Example 4) in 25 ml of dry diethyl ether in the course of 45 minutes. The reaction mixture was then stirred at a temperature of 25° C. for a further 2 hours. The resulting solid was filtered off. The filtrate was distilled under reduced pressure after addition of 0.01 g of hydroquinone monomethyl ether. 42.5 g (83 percent of theory) of 2-(4-fluorophenyl)-hexafluoro-2-propyl α-fluoroacrylate having a boiling point of 70° to 73° C. (under 0.5 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-be97bd16f5f84fe7982e4b931dce751e |
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| Source note | uspto-grants-1993_03 |
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