Tetraketopiperazine

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Tetraketopiperazine
Tetraketopiperazine.svg
Names
Preferred IUPAC name
Piperazinetetrone
Other names
2,3,5,6-Piperazinetetrone
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
UNII
  • InChI=1S/C4H2N2O4/c7-1-2(8)6-4(10)3(9)5-1/h(H,5,7,9)(H,6,8,10)
    Key: IXRCBQCSNZKFHS-UHFFFAOYSA-N
  • C1(=O)C(=O)NC(=O)C(=O)N1
Properties
C4H2N2O4
Molar mass 142.070 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetraketopiperazine is a chemical compound with a molecule containing a six member heterocyclic ring with two nitrogen atoms. Each carbon is doubly bonded to oxygen. [1]

Contents

Production

Reacting sodium oxamate (the sodium salt of oxamic acid) with hydrochloric acid yields some tetraketopiperazine. A higher yield results from reacting ethyl oxalate with sodium ethoxide. [1] Yet another way to make tetraketopiperazine is a condensation of oxamide with ethyl oxalate with sodium ethoxide present.

Excessive nitration of 2,6-diaminopyrazine ends up with tetraketopiperazine. [2]

Reactions

The nitrogen atoms in tetraketopiperazine are slightly acidic losing their hydrogen atoms as ions. Salts of tetraketopiperazine exist. Tetraketopiperazine reacts with sodium bicarbonate to yield a monosodium salt. A disodium salt results from reaction with sodium hydroxide or sodium alkoxide. These are likely to be tautomeric with a hydrogen moving to an oxygen atom. Potassium salts also exist. A monosilver salt can be made from a silver compound and a dissolved tetraketopiperazine potassium salt. Ammonia and mercury salts of tetraketopiperazine also exist. Tetraketopiperazine also can form a monohydrazone. [1]

Reduction of tetraketopiperazine yields trikeopiperazine and then 2,5-diketopiperazine. Glyoxalic acid and oxamide are side products. [3]

Properties

When heated tetraketopiperazine does not melt, but turns black at 250°C. [1]

Tetraketopiperazine is slightly soluble in water and more so in boiling acetic acid. The solid form has monoclinic prismatic crystals. [1]

pKa is 4.8 and the second pKa2 is 8.2. [3]

References

  1. 1 2 3 4 5 de Mouilpied, Alfred Theophilus; Rule, Alexander (1907). "XVI.—Tetraketopiperazine". J. Chem. Soc., Trans. 91: 176–183. doi:10.1039/CT9079100176.
  2. ↑ Bellamy, A. J.; Golding, P. (2007). "The Study of Some Potential New Synthetic Routes to LLM-105 (2,6-Diamino-3,5-dinitropyrazine 1-oxide)". Central European Journal of Energetic Materials. 4 (7): 33–57.
  3. 1 2 Owens, J.L.; Dryhurst, G. (November 1976). "Electrochemical reduction of tetraketopiperazine". Analytica Chimica Acta. 87 (1): 37–50. Bibcode:1976AcAC...87...37O. doi:10.1016/S0003-2670(01)83118-4.
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