HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606845Generated: October 31, 2026
Dimethylformamide → 2H-Perfluoroisopropyl 2-fluoroacrylate
https://huagongshe.com/reaction/1606845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 1,1,1,3,3,3-Hexafluoro-2-propanol | HCID 13529 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Fluoroacrylic acid | HCID 2782523 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2H-Perfluoroisopropyl 2-fluoroacrylate | HCID 2778359 | — |
Reaction Steps
107 g (1 mol) of the ammonium salt of α-fluoroacrylic acid are mixed with 14.5 g (0.2 mol) of dimethylformamide and 0.6 liter of xylene, and 131 g (1.1 mol) of thionyl chloride are added dropwise to the mixture in the course of one hour; the mixture is then warmed at a temperature of 80° C. for two hours. After cooling to a temperature of 0° C., a mixture of 204 g (1.1 mol) of tributylamine and 185 g (1.1 mol) of hexafluoroisopropanol is added to the reaction mixture in the course of 30 minutes. The mixture is then stirred at a temperature of 30° C. for a further hour and is finally filtered. The filtrate is distilled under a pressure of 270 mbar and hexafluoroisopropyl α-fluoroacrylate is obtained as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863236 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-09ce754421b5441c80a867e33cea86ec |
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| Source note | uspto-grants-1989_09 |
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