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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743621Generated: October 28, 2026

Sodium Chloride → 4-(Trifluoromethoxy)benzalmalononitrile

https://huagongshe.com/reaction/1743621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMalononitrileHCID 8010—
Reactantp-(Trifluoromethoxy)benzaldehydeHCID 69573—
SolventEthanolHCID 702—
SolventBenzyltrimethylammonium hydroxideHCID 66854—
Product4-(Trifluoromethoxy)benzalmalononitrileHCID 84566274%

Reaction Steps

First, 10.0 g of 4-(trifluoromethoxy)benzaldehyde and 3.50 g of malononitrile were dissolved in 60 ml of 70% (w/w) aqueous ethanol, to which a catalytic amount of benzyltrimethylammonium hydroxide was added, and the mixture was stirred at room temperature overnight. Then, a saturated aqueous sodium chloride solution was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was recrystallized from t-butyl methyl ether and hexane to give 9.24 g of (4-(trifluoromethoxy)benzylidene)malononitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07011838B2
Source datasetuspto-grants-2006_03
ORD IDord-2a5e7efdaab1403e996cb2b8a620cba8
Source noteuspto-grants-2006_03