From: David Kelly (KellyDR$##$Cardiff.ac.uk)
Date: Tue Jul 23 2002 - 11:34:59 EDT
I wish to make hexa-aminobenzene. The same literature method has
been used by all previous workers ie nucleophilic addition of ammonia
or a synthetic equivalent (eg benzylamine) to 1,3,5-tri-nitrobenzene
with in situ reoxidation, followed by reduction of the nitro groups.
HOWEVER 1,3,5-tri-nitrobenzene is a military grade explosive and
although it is reported to have low sensitivity to detonation, the safety
committee, would go ballistic (literally..............).. Has anybody got any
sharp ideas for a new synthesis. I would be prepared to tolerate no
more than two nitro groups in an intermediate.
Thanks
Dave
Dr David R. Kelly
Dept. of Chemistry, Cardiff University, PO Box 912, Cardiff, CF10
3TB, UK
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Cardiff University is the public name of the University of Wales,
Cardiff, a constituent institution of the
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