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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1388305Erstellt: 25. Oktober 2026

4-Pyridinylacetone → 4-Acetyl-3-methyl-4-(4-pyridinyl)butanenitrile

https://huagongshe.com/reaction/1388305

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-PyridinylacetoneHCID 80552—
EduktCrotononitrileHCID 637921—
EduktSodiumHCID 5360545—
EduktSodium MethoxideHCID 10942334—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Acetyl-3-methyl-4-(4-pyridinyl)butanenitrileHCID 13268971—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a stirred mixture mixture containing 59.6 g of 1-(4-pyridinyl)propanone and 100 ml of crotononitrile was added a solution of sodium methoxide in methanol obtained by adding 1 pellet of sodium shot to 20 ml of methanol. The reaction mixture was heated on a steam bath with stirring. After about 5 minutes, there was an exothermic reaction which raised the reaction temperature to 100° C. The resulting mixture was allowed to cool to room temperature and stand overnight (about 16 hours). To the reaction was added 100 ml of 10% acetic acid and 300 ml of methylene dichloride; and, the mixture was shaken well. The layers were separated and the methylene dichloride layer was dried over anhydrous magnesium sulfate and filtered. The methylene dichloride was distilled off in vacuo and the residual oil was distilled under vacuum using a small column to produce 85.0 g of 4-acetyl-3-methyl-4-(4-pyridinyl)butanenitrile, b.p. 130°-135° C. at 0.05 mm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04431651
Quelldatensatzuspto-grants-1984_02
ORD IDord-880e9e8a9a434b4982de76ed6df54d82
Quellennotizuspto-grants-1984_02