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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443580Generated: October 29, 2026

Hydrochloric Acid → 2-(2,2,3,4,4,4-Hexafluorobutyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile

https://huagongshe.com/reaction/1443580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(2,2,3,3,4,4,5,5-Octafluoropentyl)propanedinitrileHCID 25242027—
Reactant2,2,3,4,4,4-Hexafluorobutyl trifluoromethanesulfonateHCID 58879032—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(2,2,3,4,4,4-Hexafluorobutyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrileHCID 866125642.7%

Reaction Steps

1.4 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile and 3.1 g of 2,2,3,4,4,4-hexafluorobutyl trifluoromethanesulfonate were dissolved in 10 ml of ethylene glycol dimethyl ether, 0.97 g of potassium carbonate was added, and the mixture was stirred at room temperature for 7 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture, followed by extraction with methyl tert-butyl ether. The organic layer was washed successively with water, aqueous saturated sodium hydrogen carbonate and aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.06 g of 2-(2,2,3,4,4,4-hexafluorobutyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile (hereinafter, referred to as the present compound (81)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-2706cab04c864f989a3b0e4cfb207088
Source noteuspto-grants-2010_02