Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Perfluorobutyl iodide | HCID 67917 | — |
| Product | Perfluoro-2-butene | HCID 2775851 | — |
Reaction Steps
A 240 mL Hastelloy shaker tube was flushed with nitrogen, then loaded with 5 g of aluminum chlorofluoride catalyst, cooled to -78° C., evacuated and loaded with 20 g (0.06 mole) of perfluorobutyl iodide and 50 g (0.5 mole) of tetrafluoroethylene. The reaction vessel was allowed to warm and kept on a shaker at 25-30° C. at autogenous pressure. Significant pressure drop (approximately 150 psi) was observed in the first 2 hours. After 18 hours, the pressure tube was unloaded. The product, 40 g, was collected in a -78° C. cold trap. According to 19F NMR, it was a mixture of 90% of perfluorobutene-2, mixture of cis and trans isomers in a 3:2 ratio and 10% of perfluoroethyl iodide. The calculated yield of perfluorobutene-2 based on converted perfluorobutyl iodide was 72%. According to 19F NMR, the main component (about 70%) of the residue (15 g) was a mixture of perfluorohexene-2, (minor) and perfluorohexene-3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929293 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-31b31008159f439683e80044317dadba |
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| Source note | uspto-grants-1999_07 |
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