Article révisé par les pairs
Résumé : The reaction of sodium amide in liquid ammonia on 1‐methyl‐1‐benzyl‐pyrrolidinium iodide was examined and found to give two isomeric tertiary bases: one of them (yield 86%) results from a Sommelet rearrangement, the other (yield 5%) is formed through a Stevens rearrangement. Copyright © 1960 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim