A Study of the Synthesis and Amination
of 2,6-Dialkoxy-3,5-dinitropyrazines

 

 

Anthony J. BELLAMY

Cranfield University, Defence Academy of the United Kingdom,
Shrivenham, Swindon SN6 8LA, UK


Peter GOLDING
AWE Aldermaston, Reading RG7 4PR, UK

Abstract: A series of 2,6-dialkoxy-3,5-dinitropyrazines (R = Me, Et, Pr) has been
synthesized and subjected to amination. The yield and purity of the generated
2,6-diamino-3 ,5-dinitropyrazine was found to be independent of the alkoxy group
present in the precursor. This contrasts with the behaviour of 1,3,5-trialkoxy-
2,4,6-trinitrobenzene (R = Me, Et, Pr), where the purity of the 1,3,5-triamino-
2,4,6-trinitrobenzene (TATB) produced by amination was very dependent upon
the alkoxy group.

Keywords: LLM-105, 2,6-dialkoxy-3 ,5-dinitropyrazine, 2,6-dialkoxypyrazine,
nitration, amination.

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