HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluoroethylene → 2-Iodo-1,1,2,2-tetrafluoroethyl chlorosulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Product | 2-Iodo-1,1,2,2-tetrafluoroethyl chlorosulfate | HCID 11046134 | 74% |
Reaction Steps
Into a 1-liter pressure reactor was charged a mixture of iodine monochloride (390 g, 2.4 mol) and chlorosulfonic acid (490 g, 4.206 mol). The reactor was cooled and kept at 0-10° C. until 300 g of tetrafluoroethylene (3.0 mol) was added. After the addition of TFE was complete, the reaction mixture was held at 0-10° C. for 6 hr, at 25° C. for 2 hr and at 50° C. for 2 hr. The reaction mixture was then slowly poured into a large amount of ice with stirring, and worked up as described above. The desired product was obtained (610 g, 74% yield), bp. 62-64° C./6.7 kPa. 19F NMR (188.24 MHz, CDCl3): -85.6 (t, J=4.5 Hz, 2F), -65.3 (t, J=4.5 Hz, 2F). Anal. Calcd. for C2F4IClSO3 : C: 7.02, F: 22.19; Found: C: 7.19, F: 22.73.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166157 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-9f0d01de4c754affbc30daa6fa1cf67b |
| Source note | uspto-grants-2000_12 |