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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1951398Erstellt: 25. Oktober 2026

Acetic Acid → 4-(2-Acetyl-3-oxobut-1-en-1-yl)-1-naphthonitrile

https://huagongshe.com/reaction/1951398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPiperidineHCID 8082—
EduktAcetylacetoneHCID 31261—
Edukt4-Formylnaphthalene-1-carbonitrileHCID 12433009—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Acetyl-3-oxobut-1-en-1-yl)-1-naphthonitrileHCID 59603014—

Reaktionsschritte

240 mg (1.33 mmol) of 4-formyl-1-naphthonitrile, 132.6 mg (1.33 mmol) of 2,4-pentanedione, 119.3 mg (1.99 mmol) of acetic acid and 22.6 mg (0.27 mmol) of piperidine are dissolved in 20 ml of dichloromethane and heated under reflux with an inverse water trap overnight. Cooling is followed by washing twice with water, and the organic phase is dried with magnesium sulfate. The solvent is removed in a rotary evaporator and the residue is purified by column chromatography (silica gel, mobile phase: initially dichloromethane, then isohexane/ethyl acetate 3:1). The residue after concentration of the product fractions is crystallized from diethyl ether and dried under high vacuum. 340 mg (97.5% of theory) of the title compound are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08404709B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-5158365156f24d47a7465fac54d0aa45
Quellennotizuspto-grants-2013_03