And where does one get the 3-substituted cyclobutanone?
It is a very difficult precursor to make.
If anyone did happen to have a 3-substituted cyclobutanone sitting around, another use for it is as a precursor to make 1,1,3,3-tetranitrocyclobutane,
a potential high performance explosive. (The ketone functionality could be converted to an oxime, then oxidized/nitrated to a germinal di-nitro
functionality. Then the other 3-substituted group (assuming it is not a carbon atom) can be substituted with a nitro group, then oxidatively nitrated
to another germinal di-nitro functionality.) It is really quite a coincidence that you mentioned this obscure compound.
(if we compare the expected properties of this to another structurally similar explosive TNAZ, it is easy to extrapolate that it would probably be
more powerful than HMX, and also have lower sensitivity)
[Edited on 27-6-2013 by AndersHoveland]
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