The Molecular Rearrangement of Symmetrical Bis Triphenylmethylhydrazine

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ZnCli G.
Temp.
Time Min.
Found G.
Calc. G.
(CH*)j = C = N C 12 17 0. 50 0. 50 5 5 300 330 10 5 0. 005 0. 015 0. 09 0. 09 6 78. 5 17 90. 4 19 0. 61 6 330 3 0. 024 0. 11 22 . Vl'- : 21 0. 59 6 + 360 3 0. 032 0. 11 30 22 23 0. 51 0. 52 6+ 7 400 390+ 3 2 0. 030 0. 033 0. 09 0. 09 33 37 91. 3 04 0. 55 7 390+ 4 0. 031 0. 10 31 ^r 25 28 29 0. 51 0. 78 0. 57 7 7 7 390 + 450 450 2 2 0. 028 0. 038 0. 029 0. 09 0. 14 0. 10 31 27 29 approxi- mately 90 30 0. 57 7 450 ! X /6 0. 035 0. 10 35 32 0. 52 7 450 !
...1 /6 0. 031 0. 09 34 These values are calculated on the basis of the assumption (Scheme I, p. 4 of the introduction) that each molecule of hydrazine yields one molecule of aniline i not two molecules (as demanded by Scheme II).
The method used in Expts. 30 and 32 was chosen as the best under the working conditions employed. Expt. 23 gave a better yield, but 60cc, flasks of the variety which after careful annealing would stand being plunged repeatedly into a metal bath at the temperatures used were then immediately available.


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