Abstract
AbstractA convenient method to prepare 4‐formyl‐3‐arylsydone (I) from 3‐arylsydnone by the Vilsmeier reaction in moderate yields (30%‐76%) was carefully investigated.According to the Schmidt reaction, I reacts with sodium azide in concentrated sulfuric acid to produce 3‐arylsydnone‐4‐carboxamide (II). But 3‐arylsydnone‐4‐carhonitrile (III) is obtained, if dilute sulfuric acid was used instead.When III treates with concentrated sulfuric acid, II is obtained in good yield. The all possible reaction mechanisms are suggested.
Sign-in/Register to access full text options 
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.
