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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 749598Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/749598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt(4-(Trifluoromethyl)benzylidene)malononitrileHCID 714296—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
Produkt(4-(Trifluoromethyl)benzyl)malononitrileHCID 1065674351,3%

Reaktionsschritte

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)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07402691B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-d8439fc2695e4fb0b52aae099c3403eb
Quellennotizuspto-grants-2008_07