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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443584Generated: October 29, 2026

Hydrochloric Acid → 2-(4,4,5,5,5-Pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrile

https://huagongshe.com/reaction/1443584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3,3,3-Trifluoropropyl)malononitrileHCID 22185761—
Reactant4,4,5,5,5-Pentafluoropentyl trifluoromethanesulfonateHCID 86612567—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(4,4,5,5,5-Pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrileHCID 8661256820.4%

Reaction Steps

To 10 ml of ethylene glycol dimethyl ether, 6.2 g of 4,4,5,5,5-pentafluoropentyl trifluoromethanesulfonate, 1.6 g of 2-(3,3,3-trifluoropropyl)malononitrile and 1.4 g of potassium carbonate were added and the mixture was stirred at room temperature for 5 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture and the mixture was extracted with t-butyl methyl 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 0.65 g of 2-(4,4,5,5,5-pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrile (hereinafter, referred to as the present compound (89)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-d282432eb6f94f90a9b13acc5b63d3c3
Source noteuspto-grants-2010_02