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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749607Generated: October 27, 2026

Benzaldehyde → (4-(Trifluoromethylthio)benzyl)malononitrile

https://huagongshe.com/reaction/749607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantO-PhenylenediamineHCID 7243—
Reactant4-(Trifluoromethylthio)benzylidenemalononitrileHCID 22234975—
SolventEthanolHCID 702—
Product(4-(Trifluoromethylthio)benzyl)malononitrileHCID 2223499177.1%

Reaction Steps

Then, 8.00 g of (4-(trifluoromethylthio)benzylidene)malononitrile and 3.35 g of benzaldehyde were dissolved in 320 ml of ethanol, and while stirring at room temperature, 3.41 g of phenylenediamine was slowly added, and the mixture was stirred at room temperature for 5 hours. Then, the reaction mixture was concentrated, 300 ml of t-butyl methyl ether was added, and insoluble matters were filtered. The filtrate was concentrated and the resulting residue was subjected to silica gel chromatography to give 6.22 g of (4-(trifluoromethylthio)benzyl)malononitrile (the intermediate (14)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402691B2
Source datasetuspto-grants-2008_07
ORD IDord-9fb9eccb93004b279213118abb35b9b5
Source noteuspto-grants-2008_07