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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432658Erstellt: 25. Oktober 2026

Water → 4-(4-Chlorophenyl)-5-[4-(methylthio)phenyl]pentane-2,5-dione

https://huagongshe.com/reaction/432658

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CyanideHCID 8929—
Edukt4-(Methylthio)benzaldehydeHCID 76985—
Edukt4-ChlorobenzalacetoneHCID 98183—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Chlorophenyl)-5-[4-(methylthio)phenyl]pentane-2,5-dioneHCID 1875998248,3%

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

Sodium cyanide (90 mg, 1.87 mmol) was added to a solution of 4-(methylthio)benzaldehyde (300 mg, 1.97 mmol) in N,N-dimethylformamide (2 ml). While stirring the resulting mixture at 30-40° C., a solution of 4-(4-chlorophenyl)-3-buten-2-one (370 mg, 1.97 mmol) in N,N-dimethylformamide (3 ml) was dropped. The thus-obtained mixture was then stirred at the same temperature for 90 minutes. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed successively with water and brine, and was then dried over anhydrous sodium sulfate. The solvent was distilled off and the thus-obtained brown oil (762 mg) was separated and purified by preparative thin-layer chromatography on silica gel [developing solvent: hexane/diethyl ether (2/1)], whereby the title compound was obtained as a pale yellow oil (317 mg, 48.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06664256B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-7b4b4d8d6ae84cfe83233c65d3df2e74
Quellennotizuspto-grants-2003_12