HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578340Generated: October 26, 2026
Sulfur tetrafluoride → Perfluoro-3-(butoxy)propene
https://huagongshe.com/reaction/1578340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur tetrafluoride | HCID 24555 | — |
| Reactant | Heptafluorobutyroyl fluoride | HCID 67632 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Pentafluoroallyl fluorosulphate | HCID 2776028 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | Perfluoro-3-(butoxy)propene | HCID 54369168 | 64% |
Reaction Steps
A mixture of dry potassium fluoride (7.50 g, 0.13 mol), diglyme (100 ml) and heptafluorobutyroyl fluoride (prepared from the acid by treatment with sulfur tetrafluoride) (28.1 g, 0.13 mol) was stirred at 5° C. for 30 min. Perfluoroallyl fluorosulfate was added dropwise at 5° C., the mixture was stirred at this temperature for 1 hour, then at 25° C. for 3 hours. The volatile components were transferred by distillation at 40° C. (8 mm Hg), washed with water (100 ml), and distilled from a small amount of concentrated sulfuric acid to give perfluoro-3-(butoxy)propene (30.3 g, 0.083 mol, 64%) bp 80°-84° C. whose structure was confirmed by: λmax 5.57 (CF=CF2) and 7.2-9.5 μm (C-F,C-O); 19F NMR -72.1 (d J=25.2 Hz, each member t J=13.5 Hz, d J=13.5 Hz, d J=7.4 Hz) 2F, OCF2C=C, -82.1 (t J=8.1 Hz, each member m), 3F, CF3, -84.5 (m) 2F, CF2O, -92.1 (d J=52.3 Hz, each member d J=39.4 Hz, t J=7.4 Hz) 1F, cis-CF2CF2CF=CF, -105.5 (d J=117.5 Hz, each member d J=52.3 Hz, t J=25.2 Hz) 1F, trans-CF2CF=CF, -127.3 (m) 4F, CF2, and -191.0 ppm (d J=117.5 Hz, each member d J=39.4 Hz, t J=13.7 Hz, m) 1F, CF2CF=C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04292449 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-ec2db80101524c3ba16c72f75647323a |
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| Source note | uspto-grants-1981_09 |
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