Catalytic synthesis of aziridine from 1,2-diaminoethane

Authors

  • А. А. Андерсон Latvian Institute of Organic Synthesis, Riga LV-1006
  • C. П. Симонян Latvian Institute of Organic Synthesis, Riga LV-1006
  • М. B. Шиманскaя Latvian Institute of Organic Synthesis, Riga LV-1006

Abstract

The contact conversion of 1,2-diaminoethane over a tungsten trioxide catalyst at 240–580°C has been studied by an impulse chromatographic method. The basic reaction path under these conditions is unimolecular deaminocyclization to give aziridine (31–35%). Piperazine and triethylenediamine, products of bi- and trimolecular deaminocyclization, are present as products. The deamination process is accompanied by coupled dehydrogenation and hydrogenolysis reactions. Addition of the acid anhydrides SiO2, P2O5 and B2O3 to the catalyst increases its activity but has only a negligible affect on the activation energy of the process.

How to Cite
Anderson, A. A.; Simonyan, S. P.; Shimanskaya, M. V. Chem. Heterocycl. Compd. 1993, 29, 1134. [Khim. Geterotsikl. Soedin. 1993, 1324.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF00538056

Published

1993-10-25

Issue

Section

Original Papers