Abstract
Abstract We prepared p-substituted N-benzylanilinium hexafluoroantimonates, known cationic initiators, and examined their thermal reaction. The thermal reaction produced 2- or 4-benzylanilinium salts as the major products, which resulted from the rearrangement of the benzyl group. The reaction proceeded at lower temperature with higher yield when the substituent in the benzyl group was electron donating.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have