Year-end Sale % OFF 
Abstract
N-nitroso-p-toluenesulfomethylamide and N-nitroso-p-toluenesulfobenzylamide were synthesized and the behavior of their N-nitroso radical was studied. The reaction with hydrocarbons give, not nitroso compounds, but esters of p-toluenesulfonic acid by liberation of nitrogen in thermal decomposition, and, in the case of benzyl compound, formation of benzaldehyde as well.This reaction is similar to decomposition of N-nitrosoacetanilide and can well be explained by the reaction mechanism proposed for it. N-nitrososulfonamide also undergoes nitrosation reaction at temperatures below its decomposition point, e. g. forming N-nitrosodiphenylamine from diphenylamine.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
