Reduction of Azomethine Bond of Organic Compound: Part-2. Formation of Aldimine and Ketimine and their Catalytic Hydrogenation

Reduction of Azomethine Bond of Organic Compound: Part-2. Formation of Aldimine and Ketimine and their Catalytic Hydrogenation

Authors

  • C. J. Patil

DOI:

https://doi.org/10.22377/ijpba.v10i02.1788

Abstract

Azomethine compounds were prepared from Benzaldehyde and o-hydroxy-acetophenone with aniline and o-Nitroaniline. The azomethine bond in the compound is reduced using NaBH4 in 0.1 N sodium hydroxide solution. The reaction is monitored by thin-layer chromatography (TLC) and ultraviolet–visible (UV-Vis) spectral method. Etheral layer is concentrated to get the reduction product. The final products were analyzed by a physical constant, TLC, and spectral techniques such as UV-Vis and Fourier-transform infrared.

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Published

2019-05-28

How to Cite

Patil, C. J. (2019). Reduction of Azomethine Bond of Organic Compound: Part-2. Formation of Aldimine and Ketimine and their Catalytic Hydrogenation: Reduction of Azomethine Bond of Organic Compound: Part-2. Formation of Aldimine and Ketimine and their Catalytic Hydrogenation. International Journal of Pharmaceutical & Biological Archive, 10(02). https://doi.org/10.22377/ijpba.v10i02.1788

Issue

Vol. 10 No. 02 (2019): International Journal of Pharmaceutical & Biological Archive

Section

Research Articles

License

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

This is an Open Access article distributed under the terms of the Attribution-Noncommercial 4.0 International License [CC BY-NC 4.0], which requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only.