In chemistry, hexahydro-1,3,5-triazine is a class of heterocyclic compounds with the formula (CH2NR)3. Known as aldehyde ammonias, these compounds characteristically crystallize with water. They are reduced derivatives of 1,3,5-triazine, which have the formula (CHN)3, a family of aromatic heterocycles.
They are also called triazacyclohexanes or TACH's, but this acronym is also applied to cis,cis-1,3,5-triaminocyclohexane.
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Triazine
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Aromaticity: An Overview
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3,3,5-trimethylheptane
Transcription
Preparation
N,N',N''-trisubstituted hexahydro-1,3,5-triazines arise from the condensation of a primary amine and formaldehyde as illustrated by the route to 1,3,5-trimethyl-1,3,5-triazacyclohexane:
- 3 CH2O + 3 H2NMe → (CH2NMe)3 + 3 H2O
The C-substituted derivatives are obtained by reaction of aldehydes and ammonia:[1]
- 3 RCHO + 3 NH3 → (RCHNH)3 + 3 H2O
1-Alkanolamines are intermediates in these condensation reactions.[2]
The parent hexahydro-1,3,5-triazine (CH2NH)3 has been detected as an intermediate in the condensation of formaldehyde and ammonia. This reaction affords hexamethylene tetraamine.[3] The N-substituted derivatives are more stable. These
The N,N',N"-triacyltriazines are trizines with acyl groups attached to the three nitrogen centers of the ring. These triacyltriazines arise from the reaction of hexamethylene tetraamine with acid chlorides or the condensation of amides with formaldehyde.[4]
Structure
Unlike the parent triazines, the hexahydro derivatives are conformationally flexible.[5]
Related compounds and derivatives
Trimers of isocyanates are sometimes labeled as 2,4,6-trioxohexahydro-1,3,5-triazines. They have the formula (RNC(O))3 and based on the isocyanuric (trione) tautomer of cyanuric acid.
The N,N',N"-hexahydro-1,3,5-triazines function as tridentate ligands, which are called TACH (triazacyclohexanes). Examples include Mo(CO)3[(CH2)3(NMe)3] formed from the TACH ligand and molybdenum hexacarbonyl.[7]
Hexahydro-1,3,5-triazine polymers have also been synthesized.[2]
References
- ^ Nielsen, Arnold T.; Atkins, Ronald L.; Moore, Donald W.; Scott, Robert; Mallory, Daniel; LaBerge, Jeanne M. (1973). "Structure and chemistry of the aldehyde ammonias. 1-Amino-1-alkanols, 2,4,6-trialkyl-1,3,5-hexahydrotriazines, and N,N-dialkylidene-1,1-diaminoalkanes". J. Org. Chem. 38 (19): 3288–3295. doi:10.1021/jo00959a010.
- ^ a b c Garcia, J. M.; Jones, G. O.; Virwani, K.; McCloskey, B. D.; Boday, D. J.; Ter Huurne, G. M.; Horn, H. W.; Coady, D. J.; Bintaleb, A. M.; Alabdulrahman, A. M. S.; Alsewailem, F.; Almegren, H. A. A.; Hedrick, J. L. (2014). "Recyclable, Strong Thermosets and Organogels via Paraformaldehyde Condensation with Diamines". Science. 344 (6185): 732–5. Bibcode:2014Sci...344..732G. doi:10.1126/science.1251484. PMID 24833389. S2CID 28090009.
- ^ Richmond, H. H.; Myers, G. S.; Wright, George F. (1948). "The Reaction between Formaldehyde and Ammonia". Journal of the American Chemical Society. 70 (11): 3659–3664. doi:10.1021/ja01191a034.
- ^ Teeters, W. O.; Gradsten, M. A. (1950). "Hexahydro-1,3,5-tripropionyl-s-triazine". Org. Synth. 30: 51. doi:10.15227/orgsyn.030.0051.
- ^ Jewett, J. G., Breeyear, J. J., Brown, J. H., Bushweller, C. H. (2000). "Stereodynamics of 1,3,5-Trialkyl-1,3,5-triazacyclohexanes: 1H and 13C Dynamic NMR Studies. Solvent Effects. Ab Initio and Molecular Mechanics Calculations". J. Am. Chem. Soc. 122 (2): 308. doi:10.1021/ja990760d.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Tredget, Cara S.; Lawrence, Sally C.; Ward, Benjamin D.; Howe, Robert G.; Cowley, Andrew R.; Mountford, Philip (2005). "A Family of Scandium and Yttrium Tris((trimethylsilyl)methyl) Complexes with Neutral N3 Donor Ligands". Organometallics. 24 (13): 3136–3148. doi:10.1021/om050209r.
- ^ "Tricarbonyl 1,3,5‐Trimethyl‐1,3,5‐Triazacyclohexane Complexes of Chromium(0), Molybdenum(0), and Tungsten(0) M(CO)3(Me3TACH) (M = Cr, Mo, W)]". Inorganic Syntheses. 35: 109. 2010. doi:10.1002/9780470651568.ch6.
This page was last edited on 30 April 2024, at 21:56