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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743619Generated: October 25, 2026

Hydrochloric Acid → (4-(Trifluoromethyl)benzyl)malononitrile

https://huagongshe.com/reaction/1743619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(4-(Trifluoromethyl)benzylidene)malononitrileHCID 714296—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(4-(Trifluoromethyl)benzyl)malononitrileHCID 1065674351.3%

Reaction Steps

First, 4.44 g of (4-(trifluoromethyl)benzylidene)malononitrile was dissolved in 20 ml of ethanol, and while stirring at room temperature, a suspension of 0.19 g of sodium borohydride in 5 ml of ethanol was added dropwise, followed by stirring at room temperature for 30 minutes. Then, 10% hydrochloride acid was added to the reaction mixture, which became acidic and was extracted with diethyl ether. The organic layer was successively washed with 10% hydrochloric acid, a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2.30 g of (4-(trifluoromethyl)benzyl)malononitrile (the intermediate (4)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07011838B2
Source datasetuspto-grants-2006_03
ORD IDord-a93682a602b540c6aedcf7a42b38f024
Source noteuspto-grants-2006_03