HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614788Generated: October 26, 2026
Triethylamine → 2-(4-Bromophenyl)-hexafluoro-2-propyl alpha-fluoroacrylate
https://huagongshe.com/reaction/1614788
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Reactant | 2-(4-Bromophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol | HCID 23233570 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Bromophenyl)-hexafluoro-2-propyl alpha-fluoroacrylate | HCID 13980931 | 71% |
Reaction Steps
A solution of 21.5 g (0.067 mol) of 2-(4-bromophenyl)-hexafluoro-2-propanol and 6.8 g (0.067 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 8.7 g (0.08 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 3.5 hours. The resulting solid was filtered off. The filtrate was distilled under reduced pressure after addition of 0.005 g of hydroquinone monomethyl ether. 18.8 g (71 percent of theory) of 2-(4-bromophenyl)-hexafluoro-2-propyl α-fluoroacrylate having a boiling point of 66° to 69° C. (under 0.13 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-fa1dd6dbe41c431ca4743196b48bacdc |
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| Source note | uspto-grants-1993_03 |
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