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filingDate 2000-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0919027dad8cafb384d9785abdfbcedb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_001b361b14ba03c4f79cbee5b9a103a0
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publicationDate 2000-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0052011-A2
titleOfInvention Process for making 2,4,6, 8,10,12- hexanitro- 2,4,6,8,10, 12- hexa azatetracyclo [5.5.0. 0?5,9.03,11¿] -dodecane
abstract In this process 2,6,8, 12-tetraacetyl- 2,4,6,8, 10,12-hexaazatetracyclo- [5.5.0.05, 903,11]-dodecane ('TADH') is subjected to nitrolysis in the presence of a mixed acid to form HNIW. The mixed acid comprises at least one nitronium ion source (preferably nitric acid) and at least one strong acid (preferably sulfuric acid) capable of generating a nitronium ion from the source. The ratio of nitronium ion source to strong acid and the amount of TADH used are selected so that, in the event that the nitrolysis reaction is carried out at 85 °C, 99 % nitramine conversion will occur within ten minutes.
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