HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → Sodium 1,1,2,2-tetrafluoro-4-hydroxybutane-1-sulfinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromo-3,3,4,4-tetrafluorobutan-1-ol | HCID 2736369 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sodium 1,1,2,2-tetrafluoro-4-hydroxybutane-1-sulfinate | HCID 58037024 | 77% |
Reaction Steps
A 2 litter reactor was charged with 151 g (0.67 mol) of 4-bromo-3,3,4,4-tetrafluorobutan-1-ol, 600 ml of acetonitrile, 600 ml of water, 112 g (1.33 mol/2.0 equivalent)) of sodium hydrogencarbonate, and 235 g (1.35 mol/2.0 equivalent) of sodium dithionite in a nitrogen stream. The mixture was stirred at room temperature for 12 hours. The reaction solution was extracted four times with 500 ml of acetonitrile. The solvent was evaporated from the resulting organic layer to obtain 120 g of the target sodium 1,1,2,2-tetrafluoro-4-hydroxybutane-1-sulfinate. The purity of the product was 80% and the yield was 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956142B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-08d44b0454f045e3a8bd121f3569c8dd |
| Source note | uspto-grants-2011_06 |