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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 43, 2013 - Issue 21
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Original Articles

Methylsulfonic Acid Adsorbed on Silica Gel as a Solid Acid for Dimerization of Indoles: A Convenient Synthesis of 2,3′-Bi(3H-indol)-3-one Oximes

, , , &
Pages 2926-2935 | Received 08 Oct 2012, Published online: 25 Jul 2013
 

Abstract

A simple, convenient, and efficient approach for the synthesis of (E)-2,3′-bi(3H-indol)-3-one oxime derivatives has been developed. The methodology is based on a three-component coupling reaction of indoles and sodium nitrite using a silica-supported methylsulfonic acid as solid acid. The practical utility of this three-component coupling reaction has been demonstrated in the gram-scale dimerization of indole.

[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource: Full experimental and spectral details.]

GRAPHICAL ABSTRACT

ACKNOWLEDGMENTS

The authors are grateful to the NSF of China (Nos. 21162001 and 21202023), National Key Technology R&D Program of China (No. 2009BAI78B01), Jiangxi Province Key Support Program (No. 2009BNB06200), Natural Science Foundation of Jiangxi Province (No. 2009GZH0013), and Jiangxi Province Office of Education Support Program (No. GJJ10718) for financial support.

Notes

a Reaction conditions: indole (0.50 mmol), NaNO2 (0.60 mmol), rt.

b Isolated yield.

c CH3SO3H adsorbed on silica.

d Dicyclohexylamine.

a Reaction conditions: CH3SO3H-SiO2 (0.55 mmol), indole (0.50 mmol), NaNO2 (0.60 mmol), pyridine (1 mL), rt.

b Isolated yield.

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