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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443595Generated: October 29, 2026

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

https://huagongshe.com/reaction/1443595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl 5-Bromoamyl EtherHCID 14221121—
Reactant2-(3,3,3-Trifluoropropyl)malononitrileHCID 22185761—
SolventDimethyl SulfoxideHCID 679—
Product2-(5-Benzyloxypentyl)-2-(3,3,3-trifluoropropyl)malononitrileHCID 5887904481.5%

Reaction Steps

3.5 g of 2-(3,3,3-trifluoropropyl)malononitrile, 5.5 g of 5-bromopentyl benzyl ether and 0.70 g of potassium iodide were dissolved in 20 ml of dimethyl sulfoxide, 3.3 g of potassium carbonate was added, and the mixture was stirred at room temperature for 9 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 5.9 g of 2-(5-benzyloxypentyl)-2-(3,3,3-trifluoropropyl)malononitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662402B2
Source datasetuspto-grants-2010_02
ORD IDord-191b6dfc0f254c298d0b3c0ebf7af502
Source noteuspto-grants-2010_02