HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382495Generated: October 26, 2026
Potassium Hydroxide → 2,2,3,4,4,4-Hexafluorobutyl nonafluorobutane-1-sulfonate
https://huagongshe.com/reaction/2382495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | 2,2,3,4,4,4-Hexafluorobutan-1-ol | HCID 533990 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2,3,4,4,4-Hexafluorobutyl nonafluorobutane-1-sulfonate | HCID 86638305 | — |
Reaction Steps
2,2,3,4,4,4-hexafluorobutan-1-ol (202 g, 1.1 mol, obtained from Sinochem Corp., Beijing, China), 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride (332 g, 1.1 mol, obtained from 3M Company of Saint Paul, Minn.) and water (300 g) were combined in a 3-L, 3-necked round bottom flask. The flask was equipped with a magnetic stirrer, cold water condenser, thermocouple and a 250-mL addition funnel. Aqueous potassium hydroxide (149.3 g, 45 weight percent, 1.22 equivalents) was added dropwise via an addition funnel at such a rate that the temperature did not exceed 35° C. Once the addition of the base was complete the mixture was stirred for 16 hours at room temperature. The precipitated salts were then filtered from the mixture and the lower liquid fluorochemical product phase was separated from the upper aqueous phase. Unreacted 2,2,3,4,4,4-hexafluorobutan-1-ol and 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride were removed by atmospheric distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08261560B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-42f9040d960649a38fb968bcab3c1ca4 |
|---|
| Source note | uspto-grants-2012_09 |
|---|