Chemistry:1,2-Dimethylethylenediamine
From HandWiki
2.png)
| |
| Names | |
|---|---|
| Preferred IUPAC name
N,N′-Dimethylethane-1,2-diamine | |
| Other names
N,N′-Dimethyl-1,2-ethanediamine
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
| UNII | |
| |
| |
| Properties | |
| C4H12N2 | |
| Molar mass | 88.154 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.819 g/mL |
| Boiling point | 120 °C (248 °F; 393 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
1,2-Dimethylethylenediamine (DMEDA) is the organic compound with the formula (CH3NH)2C2H4. It is a colorless liquid with a fishy odor. It features two secondary amine functional groups.
Reactions
DMEDA is used as a chelating diamine for the preparation of metal complexes, some of which function as homogeneous catalysts.[1][2]
The compound is used as a precursor to imidazolidines by condensation with ketones or with aldehydes:
- RR'CO + C2H4(CH3NH)2 → C2H4(CH3N)2CRR' + H2O
2Cl2frag.png)
View down chelate ring-Ni axis in trans-[NiCl2(DMEDA)2] (one DMEDA and chloride ligands omitted for clarity).[3] Color code: green = Ni, violet = N, dark gray = C
See also
References
- ↑ Chan, Timothy R.; Hilgraf, Robert; Sharpless, K. Barry; Fokin, Valery V. "Polytriazoles as copper(I)-stabilizing ligands in catalysis" Organic Letters 2004, volume 6, 2853-2855. doi:10.1021/ol0493094
- ↑ Klapars, Artis; Huang, Xiaohua; Buchwald, Stephen L. (2002). "A General and Efficient Copper Catalyst for the Amidation of Aryl Halides". Journal of the American Chemical Society 124 (25): 7421–7428. doi:10.1021/ja0260465. PMID 12071751.
- ↑ Ariyananda, W. G. Piyal; Norman, Richard E. (2006). "trans-Dichlorobis(N,N'-dimethylethane-1,2-diamine-κ2N,N')nickel(II)". Acta Crystallographica Section E 62: m2339–m2341. doi:10.1107/S1600536806033770.
 |  |
