HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206965Generated: October 30, 2026
Tetrafluoroethylene → Ethanesulfonic acid, 1,1,2,2-tetrafluoro-, sodium salt (1:1)
https://huagongshe.com/reaction/2206965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethanesulfonic acid, 1,1,2,2-tetrafluoro-, sodium salt (1:1) | HCID 87303205 | 32.7% |
Reaction Steps
The sodium sulphite (201 g) was dissolved in water (600 mL) and taken in a 1000 mL Hastelloy reactor. Tetrafluoroethylene (150 g) was added to the reactor at −130° C. The temperature of the reactor was increased to 120° C. and maintained at 120° C. for 12 hours. The reactor was cooled to 25° C. and unreacted tetrafluoroethylene was vented off. The water of the reaction was removed from reaction mixture by azeotropic distillation to obtain a reaction mass. The reaction mass was extracted with hot ethanol using soxhlet apparatus. The ethanolic solution was concentrated to obtain pure sodium tetrafluoroethane sulfonate (100 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376379B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-429142376b494d088084b38f5ed80ddc |
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| Source note | uspto-grants-2016_06 |
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