N-Alkylation of amines with alcohols over nanosized zeolite beta was written by Reddy, Marri Mahender;Kumar, Macharla Arun;Swamy, Peraka;Naresh, Mameda;Srujana, Kodumuri;Satyanarayana, Lanka;Venugopal, Akula;Narender, Nama. And the article was included in Green Chemistry in 2013.Formula: C14H12N2 This article mentions the following:
Direct N-alkylation of amines with alcs. was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure. The catalyst was successfully recovered and reused without significant loss of activity and only water is produced as co-product. In addition, imines were also efficiently prepared from the tandem reactions of amines with 2-, 3- and 4-nitrobenzyl alcs. using nanosized zeolite beta. In the experiment, the researchers used many compounds, for example, 4-(Benzylamino)benzonitrile (cas: 10282-32-3Formula: C14H12N2).
4-(Benzylamino)benzonitrile (cas: 10282-32-3) belongs to nitriles. Nitrile compounds can be prepared by the incorporation of a cyanide source through C–C bond formation or by dehydration of primary carboxamides. Nitrile groups in organic compounds can undergo a variety of reactions depending on the reactants or conditions. A nitrile group can be hydrolyzed, reduced, or ejected from a molecule as a cyanide ion.Formula: C14H12N2
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts