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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443565Generated: October 29, 2026

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

https://huagongshe.com/reaction/1443565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant(2,2,3,3,4,4,5,5-Octafluoropentyl)propanedinitrileHCID 25242027—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-Bromopropyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrileHCID 8661255169.8%

Reaction Steps

3.2 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile and 8.6 g of 1,3-dibromopropane were dissolved in 20 ml of dimethyl sulfoxide, 3.0 g of potassium carbonate was added, and the mixture was stirred at room temperature for 2 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 3.2 g of 2-(3-bromopropyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile (hereinafter, referred to as the present compound (65)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-4e035ce0af4b4b2bba975d93fb4a1d23
Source noteuspto-grants-2010_02