Organic Chemistry: Current Research
Open Access

Chemo selective reactions of Diaminomaleonitrile (DAMN) in water

2^nd International Conference on Past and Present Research Systems of Green Chemistry

September 14-16, 2015 Orlando, USA

Jicli Jos�© Rojas1, Augusto Rivera1, Jaime R�­osâ��Motta1 and Francisco Le�³n2

1Universidad Nacional de Colombia, Colombia 2The University of Mississippi, USA

Posters-Accepted Abstracts: Organic Chem Curr Res

Abstract :

Diaminomaleonitrile (DAMN) is one of the most versatile reagents in Organic Chemistry. It has been used as a precursor for producing nucleotides and for synthesizing a wide variety of heterocyclic compounds including purines, pyrimidines, pyrazines (some which are widely employed in the fluorescent dye industry), imidazoles, biphenylenes, porphyrazines (which have great potential in optical sensor technology) and diimines that are used as catalysts. The reaction of DAMN with aromatic aldehydes is widely known to produce monoimines which are important as synthetic intermediates in the synthesis of drugs, conjugated linear polymers and in the thermostable optical material industry. Most reaction methods described involve the use methanol as a solvent without catalysts, but ethanol and acid catalysis are required if the aldehyde bears a strong electron-withdrawing group. Earlier in our laboratory we have sought to apply green chemistry principles to the reaction between DAMN and various aromatic aldehydes employing either water as solvent without catalysts or under solvent-free conditions, thus obtaining the respective monoimines. The reactions carried out in water were also shown to be chemo-selective. The fact that water was used as solvent in this type of reaction makes this a cleaner, more efficient and attractive method for preparing this type of substances.

Biography :

Email: rsjiclij@unal.edu.co