2,4,6-Trimethylaniline
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| Names | |||
|---|---|---|---|
| IUPAC name
2,4,6-Trimethylaniline | |||
| Other names
Aminomesitylene; 2,4,6-Trimethylbenzenamine; Mesitylamine; Mesidine | |||
| Identifiers | |||
88-05-1  | |||
| ChemSpider | 6647 | ||
| Jmol interactive 3D | Image | ||
| KEGG | C19540 | ||
| PubChem | 6913 | ||
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| Properties | |||
| C9H13N | |||
| Molar mass | 135.21 g/mol | ||
| Density | 0.963 g/mL | ||
| Boiling point | 233 °C (451 °F; 506 K) | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
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| Infobox references | |||
2,4,6-Trimethylaniline is a organic compound with formula (CH3)3C6H2NH2. It is an aromatic amine that is of commercial interest as a precursor to dyes. It is prepared by selective mononitration of mesitylene, avoiding oxidation of the methyl groups. The resulting nitro compound is reduced to the aniline.[1]
Coordination chemistry
Trimethylaniline is a building block to a variety of bulky ligands. Condensation with glyoxal gives the 1,2-diimine ligands. An example is glyoxal-bis(mesitylimine), a yellow solid that is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal. The diimine is a useful precursor to popular NHC ligands including IMes.[2] N-heterocyclic carbenes, as found in 2nd generation Grubbs' catalyst, are also prepared from this compound.[3]
A substituted 1,2-diimine ligand and an idealized metal complex.
Condensation with 1,3-diketones gives NacNac ligands.
References
- ↑ Gerald Booth "Nitro Compounds, Aromatic" in "Ullmann's Encyclopedia of Industrial Chemistry" 2007; Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_411
- ↑ Elon A. Ison, Ana Ison "Synthesis of Well-Defined Copper N-Heterocyclic Carbene Complexes and Their Use as Catalysts for a “Click Reaction”: A Multistep Experiment That Emphasizes the Role of Catalysis in Green Chemistry" J. Chem. Educ., 2012, volume 89, pp 1575–1577. doi:10.1021/ed300243s
- ↑ Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. (1999). "Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands". Organic Letters 1 (6): 953–956. doi:10.1021/ol990909q.