One-Pot Synthesis of β-Amino Ketones via Direct Mannich-type Reaction Catalyzed with CuFe2O4@SO3H
محل انتشار: بیست و ششمین سمینار شیمی آلی ایران
سال انتشار: 1397
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 246
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شناسه ملی سند علمی:
ISOC26_069
تاریخ نمایه سازی: 2 شهریور 1398
چکیده مقاله:
Mannich reactions are among the most important carbon–carbon bond forming reactions inorganic synthesis. They provide β-amino carbonyl compounds, which are important syntheticintermediates for various pharmaceuticals and natural products [1]. Therefore, the developmentof new synthetic methods leading to β-amino carbonyl compounds or their derivativeshas attracted much attention. However, the classic Mannich reaction has limited applications.Attempts have been made in the past to improve methodologies based on two-component reactions,where the imine as electrophile is formed and then reacted with nucleophiles such asenolates, enol ethers, and enamines [2]. However, in most cases these protocols use hazardousorganic solvents, costly and non-recoverable catalysts, and requirement of special effort forcatalyst preparation, and suffer from long reaction time with low yields [3]. Therefore, thedevelopment of modern versions of the reaction that work under mild conditions is of greatimportance. CuFe2O4@SO3H is an excellent acidic catalyst, which is frequently used to promotesome important reactions. We report herein full details of a novel, convenient, and simpleprocedure to realize a one-pot three-component reaction of aldehydes, amines, and ketones,catalyzed by CuFe2O4@SO3H, for the preparation of β-amino carbonyl compounds inEtOH.
نویسندگان
Fahimeh Assadzadeh
Department of Chemistry, Faculty of Sciences, University of Birjand, Birjand, Iran
Mohammad Ali Nasseri
Department of Chemistry, Faculty of Sciences, University of Birjand, Birjand, Iran
Seyyedeh Ameneh Alavi Gol
Department of Chemistry, Faculty of Sciences, University of Birjand, Birjand, Iran