Journal :   Asian Journal of Research in Chemistry

Volume No. :   4

Issue No. :  2

Year :  2011

Pages :   285-288

ISSN Print :  0974-4169

ISSN Online :  0974-4150


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Synthesis of Biphenylamine Derivatives via Suzuki Coupling Reaction



Address:   R. Margabandu and K. Subramani*
1Department of Chemistry, Islamiah College, Vaniyambadi, PIN- 635751, Tamil Nadu, India
*Corresponding Author
DOI No:

ABSTRACT:
The biphenyl amine derivatives has been prepared via suzuki coupling, oxidation of sulfide to sulfonyl and reductive amination. The palladium tetrakistriphenylphosphine was used as a catalyst in suzuki coupling. The sodium periodate and sodium triacetoxyborohydride are used as reagent in oxidation and reductive amination reactions. The intermediates are confirmed by corresponding functional peak in IR spectrum and characterization of final product were done with help of IR, 1H NMR and mass spectral data.
KEYWORDS:
Suzuki coupling, Pd (0) complex, IR, NMR and Mass.
Cite:
R. Margabandu, K. Subramani. Synthesis of Biphenylamine Derivatives via Suzuki Coupling Reaction. Asian J. Research Chem. 4(2): February 2011; Page 285-288.
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