Pyrazinium Di(hydrogen sulfate) as a Novel, Highly Efficient and Homogeneous Catalyst for the Condensation of Enolizable Ketones with Aldehydes, Acetonitrile and Acetyl Chloride

A highly efficient protocol for the synthesis of β‐acetamido ketone or ester derivatives in the presence of pyrazinium di(hydrogen sulfate) {Py(OSO3H)2} as a novel, green and homogeneous solid acid catalyst at room temperature is described. One‐pot multi‐component condensation of enolizable ketones...

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Veröffentlicht in:Journal of the Chinese Chemical Society (Taipei) 2012-02, Vol.59 (2), p.199-207
Hauptverfasser: Khazaei, Ardeshir, Zolfigol, Mohammad Ali, Mokhlesi, Mohammad, Zare, Abdolkarim, Derakhshan-Panah, Fatemeh, Merajoddin, Maria, Keypour, Hassan, Dehghani-Firouzabadi, Ahmad Ali
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Sprache:eng
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Zusammenfassung:A highly efficient protocol for the synthesis of β‐acetamido ketone or ester derivatives in the presence of pyrazinium di(hydrogen sulfate) {Py(OSO3H)2} as a novel, green and homogeneous solid acid catalyst at room temperature is described. One‐pot multi‐component condensation of enolizable ketones or alkyl acetoacetates with aldehydes, acetonitrile and acetyl chloride affords the title compounds in high to excellent yields and in relatively short reaction times. In this work, the efficiency of our recently reported solid acid catalyst, saccharin sulfonic acid (Sa‐SO3H), in the synthesis of β‐acetamido ketones/esters is also studied. Moreover, in this research, some new β‐acetamido ketones and esters (i.e. one complex structure) are prepared. A highly efficient protocol for the synthesis of β‐acetamido ketone or ester derivatives in the presence of pyrazinium di(hydrogen sulfate) {Py(OSO3H)2} as a novel, green and homogeneous solid acid catalyst (or saccharin sulfonic acid) at room temperature is described. one‐pot multi‐component condensation of enolizable ketones or alkyl acetoacetates with aldehydes, acetonitrile and acetyl chloride affords the title compounds in high yields and short reaction times.
ISSN:0009-4536
2192-6549
DOI:10.1002/jccs.201100383