Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 2117 - 2122 (1989)
Update date:2022-08-05
Topics:
Abdrakhmanov, I. B.
Saraeva, Z. N.
Nigmatullin, N. G.
Komissarov, V. D.
Tolstikov, G. A.
A series of 4-R2-N-R1-N-(1-methyl-2-butenyl)- and 4-R2-N-R1-2-(1-methyl-2-butenyl)-anilines was synthesized.The rate constants of rearrangement and elimination of the hydrochlorides of the 4-R2-N-R1-N-(1-methyl-2-butenyl)anilines in nitrobenzene were measured at 110 and 130 deg C.The correlation equations which describe the effect of the nature of the substituents on the reactivity of the substrate in these reactions and the selectivity of their occurence were established.A mechanism of the processes was proposed.
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