HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178835Generated: October 25, 2026
Trifluoroacetyl fluoride → 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene
https://huagongshe.com/reaction/1178835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetyl fluoride | HCID 67716 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene | HCID 85887656 | 31% |
Reaction Steps
Trifluoroacetyl fluoride (6 g, 0.051 mole) is bubbled into a mixture of KF (2.4 g, 0.041 mole) and dry diglyme (15 ml). The reaction mixture is stirred at 20° C. for 30 minutes and then CH2═C(CF3)CF2OSO2F (10 g, 0.041 mile) is added gradually. The resulting mixture is stirred at 20° C. for 1 hour. Hexafluoroisobutylene is distilled from the reaction mixture and the residue is poured into water. The organic layer is separated, washed in turn with aqueous sodium bicarbonate solution and water, and then dried over MgSO4. Distillation gives 3,3-Difluoro-3-pentafluoroethoxy-2-trifluoromethylpropene (CH2═C(CF3)CF2OCF2CF3) (3.5 g, 31% yield, b.pt. 67° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276624B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-134a76217b16465c8f4d7d8c2b11e39d |
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| Source note | uspto-grants-2007_10 |
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