p-Toluene Sulfonic Acid Catalyzed One-Pot Synthesis of Unsymmetrical 1,4-Dihydropyridines Derivatives via Hantzsch Reaction
Corresponding Author(s) : Hua-Nan Peng
huananpeng@126.com
Asian Journal of Chemistry,
Vol. 23 No. 4 (2011): Vol 23 Issue 4
Abstract
A simple, inexpensive and efficient one-pot synthesis of a series of unsymmetrical 1,4- dihydropyridines derivatives using p-toluene sulfonic acid as catalyst at room temperature was achieved in excellent yields from the four-component Hantzsch condensation reactions of various aromatic aldehydes, 1,3-cyclohexanedione, methyl acetoacetate (or ethyl acetoacetate) and ammonium acetate in a little methanol (or ethanol). The procedure possesses the advantages of short reaction time, high yields, an environmental friendly procedure as well as easy isolation of products.
Keywords
p-Toluene sulfonic acid
Hantzsch condensation reaction
1,4-Dihydropyridine
Peng, H.-N., Peng, X.-M., & Zheng, D.-G. (2010). p-Toluene Sulfonic Acid Catalyzed One-Pot Synthesis of Unsymmetrical 1,4-Dihydropyridines Derivatives via Hantzsch Reaction. Asian Journal of Chemistry, 23(4), 1833–1837. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/10267
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