HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276566Generated: November 1, 2026
Tetrafluoroethylene → 1,1,2,2-Tetrafluoro-2-iodoethyl sulfurofluoridate
https://huagongshe.com/reaction/1276566
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Fluorosulfuric acid | HCID 24603 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Product | 1,1,2,2-Tetrafluoro-2-iodoethyl sulfurofluoridate | HCID 12596365 | 66% |
Reaction Steps
Into a 1-liter pressure reactor was charged a mixture of iodine monochloride (162.5 g, 1.0 mol) and fluorosulfonic acid (110 g, 1.1 mol). The reactor was cooled and tetrafluoroethylene (120 g, 1.2 mol) was added. After the addition of TFE was complete, the reaction mixture was heated at 100° C. for 10 hr. The cooled mixture was then slowly poured into a large amount of ice with stirring. The lower layer was separated, washed with dilute NaHSO3 solution and water and dried over MgSO4. Distillation afforded the desired product as a clear liquid (215 g, 66% yield), bp. 87-88° C. 19F NMR (188.24 MHz, CDCl3): -85.4 (dt, J=8.4 Hz, J=5.2 Hz, 2F), -65.7 (t, J=5.2 Hz, 2F), +49.6 (t, J=8.3 Hz, 1F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166157 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-61e4a0a666194caf8b154a89b30b167f |
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| Source note | uspto-grants-2000_12 |
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