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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443563Generated: October 29, 2026

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

https://huagongshe.com/reaction/1443563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3-DibromobutaneHCID 7889—
ReactantPotassium CarbonateHCID 11430—
Reactant(2,2,3,3,4,4,5,5-Octafluoropentyl)propanedinitrileHCID 25242027—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-Bromobutyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrileHCID 8661254957.8%

Reaction Steps

1.4 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile and 2.2 g of 1,3-dibromobutane were dissolved in 10 ml of dimethyl sulfoxide, 0.83 g of potassium carbonate was added, and the mixture was stirred at room temperature for 4 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 1.2 g of 2-(3-bromobutyl)-2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile (hereinafter, referred to as the present compound (62)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-f59c9c6428a94b4b8735261a8079ea6d
Source noteuspto-grants-2010_02