Abstract
The susceptibility constants measured for the reaction of 3-bromo-(Ia) and 3-methoxy-2-thenoyl (Ic) chlorides with some meta- and para-substituted anilines in benzene at 25°C have confirmed the occurrence of two different mechanisms for the anilinodechlorination of 3-substituted 2-thenoyl chlorides: (i) the classical AE mechanism and (ii) the IP mechanism (unusual for reactions with anilines in nonpolar aprotic solvents) which can operate when electron-releasing substituents are present in the thiophen ring.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
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 call
