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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 43, 2013 - Issue 17
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Original Articles

Efficient Synthesis of Symmetrical Bisamides from Aldehydes and Amides Catalyzed by Silica-Bonded S-Sulfonic Acid Nanoparticles

, , &
Pages 2370-2379 | Received 17 Apr 2012, Published online: 03 Jun 2013
 

Abstract

Silica-bonded S-sulfonic acid nanoparticles (SBSSANPs) were easily synthesized from silica nanoparticles and showed to be an efficient catalyst in the synthesis the symmetrical N,N′-alkylidene bisamides. Reaction of aldehydes and amides in the presence of the catalyst afforded the corresponding bisamides in good to excellent yields. The extensive range of substrates suggests general applicability of the method. Reusability of the catalyst, simple workup procedure, and short reaction times are other advantages of this protocol.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications ® to view the free supplemental file.

GRAPHICAL ABSTRACT

ACKNOWLEDGMENT

We are thankful to the Research Council of Mazandaran University for the partial support of this work.

Notes

a Isolated yield.

b SiO2 with 12.6-nm average particle size.

c Non-nanoparticle silica-bonded S-sulfonic acid.

a The reaction was carried out in 7 mL of solvent at reflux.

b Isolated yield.

c The reaction was carried out at 100 °C.

a Optimized conditions: aldehyde (1 mmol), amide (2 mmol), SBSSANPs (0.08 g), and toluene at reflux temperature.

b Isolated yield.

a Reaction conditions: aldehyde (1 mmol), acetamide (1 mmol), benzmide (1 mmol), SBSSANPs (0.08 g), and toluene at reflux.

b Ratio determined by 1H NMR analysis.

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