Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Reactant | HCID 53435538 | HCID 53435538 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13980932 | HCID 13980932 | 73.3% |
Reaction Steps
A solution of 21 g (0.081 mol) of 2-tolylhexafluoro-2-propanol and 8.2 g (0.08 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 40 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 0.02 g of hydroquinone monomethyl ether. 19.6 g (73 percent of theory) of 2-tolylhexafluoro-2-propyl α-fluoroacrylate having a boiling point of 58° to 60° C. (under 0.27 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-a61da22a3e78431ba545cb9f6cd1c420 |
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| Source note | uspto-grants-1994_06 |
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