HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991273Generated: November 1, 2026
Sodium Sulfite → Sodium 1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfinate
https://huagongshe.com/reaction/991273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium perfluorobutanesulfonate | HCID 23678450 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Sodium 1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfinate | HCID 23671909 | 65% |
Reaction Steps
A three necked 500 ml reaction flask, equipped with a reflux condenser, a stirrer, a thermometer and a heating mantle was charged with 30.2 g of C4F9SO2F (0.1 moles), 15.1 g Na2SO3 (0.12 moles), 16.8 g NaHCO3 (0.2 moles), 50 g EtOH and 50 g DI-water. The reaction mixture was degassed 3 times using nitrogen and aspirator vacuum. The mixture was then heated to 60° C. under a nitrogen atmosphere for 16 hours. A slightly yellow reaction mixture with a pH of 6.5 was obtained. EtOH was stripped off under reduced pressure using an aspirator vacuum (20 torr and temperature between 60-85° C.) and the temperature was kept below 110° C. in order to avoid thermal decomposition of the sulfinate product. 19F analysis indicated a yield of 65% sodium perfluorobutyl sulfinate and 25% sodium perfluorobutyl sulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06462228B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3ff024aa334849edbe9ba11293eb891e |
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| Source note | uspto-grants-2002_10 |
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