5-Aminotetrazole

5-Aminotetrazole
Names
Preferred IUPAC name
1H-1,2,3,4-Tetrazol-5-amine
Other names
5-ATZ
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.022.348 Edit this at Wikidata
UNII
  • InChI=1S/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)
    Key: ULRPISSMEBPJLN-UHFFFAOYSA-N
  • InChI=1/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)
    Key: ULRPISSMEBPJLN-UHFFFAOYAD
  • c1([nH]nnn1)N
Properties
CH3N5
Molar mass 85.070 g·mol−1
Appearance White solid
Density 1.502 g/cm3
Melting point 201–205 °C (394–401 °F; 474–478 K)
Hazards
GHS labelling:
GHS02: FlammableGHS05: Corrosive
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

5-Aminotetrazole is an organic compound with the formula HN4CNH2. It is a white solid that can be obtained both in anhydrous and hydrated forms.

The molecule is planar.[1] The hydrogen bonding pattern in the hydrate supports the assignment of NH being adjacent to carbon in the ring.[2]

Preparation

[edit]

A synthesis of 5-aminotetrazole through the action of nitrous acid on aminoguanidine was reported by Johannes Thiele in 1892.[3]

The exact structure of the compound was not known at the time, although it was known to crystallize as a monohydrate. The correct structural formula was published in 1901 by Arthur Hantzsch, who obtained it from the reaction between cyanamide and hydrazoic acid.[4]

To avoid direct handling of the problematic hydrazoic acid, a mixture of sodium azide and hydrochloric acid has been used to give the monohydrate at 73% yield.[5]

In a more efficient and controllable one-pot synthesis, cyanamide is treated with hydrazine hydrochloride to give aminoguanidine hydrochloride, which is then diazotized as in Thiele's original process. Addition of ammonia or sodium hydroxide followed by heat-induced cyclization gives the anhydrous product in 74% yield.[6][7]

Structure

[edit]

The structure of 5-aminotetrazole has been determined several times by X-ray crystallography, both as the anhydrous[8] and monohydrated forms.[9] The structures are very similar, consisting of a planar molecule, including the amino group.

Uses

[edit]

5-Aminotetrazole has found applications in heterocyclic chemistry, particularly as a synthon for some multicomponent reactions.[10]

The N-4 is basic as indicated by its binding to metal halides, such as the coordination complex [CoCl2(aminotetrazole)4.[11]

The compound has a particularly high nitrogen content of 80%. Partly for this reason, the compound is prone to decomposition to nitrogen gas (N2). It has been widely investigated for gas-generating systems, such as airbags and blowing agents.[12]

References

[edit]
  1. ^ Hiroshi Fujihisa, Kazumasa Honda, Shigeaki Obata, Hiroshi Yamawaki, Satoshi Takeya, Yoshito Gotoha, Takehiro Matsunaga "Crystal structure of anhydrous 5-aminotetrazole and its high-pressure behavior" CrystEngComm, 2011, volume 13, pp. 99-102. doi:10.1039/C0CE00278J
  2. ^ D. D. Bray and J. G. White "Refinement of the structure of 5-aminotetrazole monohydrate" Acta Crystallogr. (1979). B35, pp. 3089-3091.doi:10.1107/S0567740879011493
  3. ^ Thiele, Johannes (1892-01-01). "Ueber Nitro- und Amidoguanidin". Justus Liebigs Annalen der Chemie. 270 (1–2): 1–63. doi:10.1002/jlac.18922700102. ISSN 0075-4617.
  4. ^ Hantzsch, A.; Vagt, A. (1901-01-01). "Ueber das sogenannte Diazoguanidin". Justus Liebigs Annalen der Chemie. 314 (3): 339–369. doi:10.1002/jlac.19013140307. ISSN 0075-4617.
  5. ^ MIHINA, JOSEPH S.; HERBST, ROBERT M. (1950-09-01). "The Reaction of Nitriles with Hydrazoic Acid: Synthesis of Monosubstituted Tetrazoles". The Journal of Organic Chemistry. 15 (5): 1082–1092. doi:10.1021/jo01151a027. ISSN 0022-3263.
  6. ^ US 5424449, Rothgery, Eugene F. & Knollmueller, Karl O., "Process for the preparation of 5-aminotetrazole", published 1995-06-13, issued 1995-06-13 
  7. ^ US 5594146, Murotani, Masahiro; Mura, Hajime & Takeda, Makoto et al., "Process for producing 5-aminotetrazole", published 1997-01-14, issued 1997-01-14 
  8. ^ Fujihisa, Hiroshi; Honda, Kazumasa; Obata, Shigeaki; Yamawaki, Hiroshi; Takeya, Satoshi; Gotoh, Yoshito; Matsunaga, Takehiro (2011). "Crystal structure of anhydrous 5-aminotetrazole and its high-pressure behavior". CrystEngComm. 13: 99–102. doi:10.1039/c0ce00278j.
  9. ^ Bray, D. D.; White, J. G. (1979). "Refinement of the structure of 5-aminotetrazole monohydrate". Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 35 (12): 3089–3091. Bibcode:1979AcCrB..35.3089B. doi:10.1107/S0567740879011493.
  10. ^ Dolzhenko, A. V. (2017). "5-Aminotetrazole as a Building Block for Multicomponent Reactions (Review)". Heterocycles. 94 (10): 1819–1846. doi:10.3987/rev-17-867.
  11. ^ Zhao, Fang-Hua; Che, Yun-Xia; Zheng, Ji-Min; Grandjean, Fernande; Long, Gary J. (2012). "Two Acentric Mononuclear Molecular Complexes with Unusual Magnetic and Ferroelectric Properties". Inorganic Chemistry. 51 (8): 4862–4868. doi:10.1021/ic300394c. PMID 22480292.
  12. ^ Lesnikovich, A. I.; Ivashkevich, O. A.; Levchik, S. V.; Balabanovich, A. I.; Gaponik, P. N.; Kulak, A. A. "Thermal decomposition of aminotetrazoles" Thermochimica Acta 2002, vol. 388, pp. 233-251. doi:10.1016/S0040-6031(02)00027-8
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