An Efficient Metal-Free Method for the Denitrosation of Aryl N-Nitrosamines at Room Temperature was written by Chaudhary, Priyanka;Korde, Rishi;Gupta, Surabhi;Sureshbabu, Popuri;Sabiah, Shahulhameed;Kandasamy, Jeyakumar. And the article was included in Advanced Synthesis & Catalysis in 2018.Related Products of 10282-32-3 This article mentions the following:
A simple and practical method for the denitrosation of aryl N-nitrosamines to secondary amines is reported under metal-free conditions using iodine and triethylsilane. Several reduction-susceptible functional groups such as alkene, alkyne, nitrile, nitro, aldehyde, ketone and ester are very stable during the denitrosation, which is remarkable. Broad substrate scope, room temperature reactions and excellent yields are the addnl. features of the current methodol. In the experiment, the researchers used many compounds, for example, 4-(Benzylamino)benzonitrile (cas: 10282-32-3Related Products of 10282-32-3).
4-(Benzylamino)benzonitrile (cas: 10282-32-3) belongs to nitriles. The electronic structure of nitriles is very similar to that of an alkyne with the main difference being the presence of a set of lone pair electrons on the nitrogen. Alkyl nitriles are sufficiently acidic to undergo deprotonation of the C-H bond adjacent to the CN group.Strong bases are required, such as lithium diisopropylamide and butyl lithium. The product is referred to as a nitrile anion. Related Products of 10282-32-3
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts