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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421455Generated: November 2, 2026

Acetonitrile → Sodium 1,1,2,2-tetrafluoro-4-hydroxybutane-1-sulfinate

https://huagongshe.com/reaction/2421455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-3,3,4,4-tetrafluorobutan-1-olHCID 2736369—
SolventWaterHCID 962—
ProductSodium 1,1,2,2-tetrafluoro-4-hydroxybutane-1-sulfinateHCID 5803702477%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956142B2
Source datasetuspto-grants-2011_06
ORD IDord-08d44b0454f045e3a8bd121f3569c8dd
Source noteuspto-grants-2011_06