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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1951395Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1951395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPiperidineHCID 8082—
EduktAcetylacetoneHCID 31261—
Edukt4-Formyl-3-methylbenzonitrileHCID 10909695—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methylbenzonitrileHCID 59603030—

Reaktionsschritte

950 mg (6.54 mmol) of 3-methyl-4-formylbenzonitrile [S. Levesque et al., Bioorg. Med. Chem. Lett. 11, 3161-3164 (2000], 655.2 mg (6.544 mmol) of 2,4-pentanedione, 589.5 mg (9.82 mmol) of acetic acid and 111.5 mg (1.31 mmol) of piperidine are dissolved in 35 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). After concentration of the product fractions, the residue is crystallized from diethyl ether and dried under high vacuum. 1.12 g (75.3% of theory) of the title compound are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08404709B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-ffc25bb006974dd58b30decbfe449b09
Quellennotizuspto-grants-2013_03