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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443561Generated: October 30, 2026

Hydrochloric Acid → HCID 86612547, compound

https://huagongshe.com/reaction/1443561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(3,3,3-Trifluoropropyl)malononitrileHCID 22185761—
SolventTetrahydrofuranHCID 8028—
SolventTetrabutylammonium FluorideHCID 2724141—
Solvent2-chloro-3,3,3-trifluoroprop-1-eneHCID 2736716—
ProductHCID 86612547HCID 86612547—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.6 g of 2-(3,3,3-trifluoropropyl)malononitrile was dissolved in 20 ml of a solution (1 mol/L) of tetrabutylammonium fluoride in tetrahydrofuran, 5 ml of 2-chloro-3,3,3-trifluoropropene was added thereto at 0° C., and the mixture was stirred at room temperature for 3 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 0.22 g of 2-(2-chloro-3,3,3-trifluoropropyl)-2-(3,3,3-trifluoropropyl)malononitrile (hereinafter, referred to as the present compound (58)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-a05ec5c8c1054e76b1009af982424a5b
Source noteuspto-grants-2010_02