Dimedone

Dimedone
Names
	IUPAC name 5,5-Dimethylcyclohexane-1,3-dione
	Other names Cyclomethone,; 5,5-dimethyl-1,3-cyclohexanedione,; Dimethyldihydroresorcinol,; Methone
Identifiers
CAS Number	126-81-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	29091 ;
ECHA InfoCard	100.004.369
PubChem CID	31358;
CompTox Dashboard (EPA)	DTXSID8021987 ;
	InChI InChI=1S/C8H12O2/c1-8(2)4-6(9)3-7(10)5-8/h3-5H2,1-2H3 Key: BADXJIPKFRBFOT-UHFFFAOYSA-N ; InChI=1/C8H12O2/c1-8(2)4-6(9)3-7(10)5-8/h3-5H2,1-2H3 Key: BADXJIPKFRBFOT-UHFFFAOYAX;
	SMILES O=C1CC(=O)CC(C)(C)C1;
Properties
Chemical formula	C8H12O2
Molar mass	140.17968
Appearance	Yellow crystals
Melting point	147 to 150 °C (297 to 302 °F; 420 to 423 K) (decomposes)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Dimedone is a cyclic diketone used in organic chemistry to determine whether a compound contains an aldehyde group. Cyclohexanediones in general can be used as catalysts in the formation of transition-metal complexes. Other uses include applications in colorimetry, crystallography, luminescence and spectrophotometric analysis. It can also be used for chemistry involving organic compounds of low electrical resistance.

Synthesis

Dimedone is prepared from mesityl oxide and dimethyl malonate.^[1]

Physical properties

Dimedone usually comes in the form of white crystals. It is stable under ambient conditions and soluble in water, as well as ethanol and methanol. It has a melting point range of 147–150 °C (420–423 K).

Tautomerism

Dimedone is in equilibrium with its tautomer in solution — in a 2:1 keto to enol ratio in chloroform.^[2]

Crystalline dimedone contains chains of molecules, in the enol form, linked by hydrogen bonds:^[3]

References

^ R. L. Shriner and H. R. Todd (1935). "5,5-dimethyl-1,3-cyclohexanedione". Organic Syntheses. 15: 16. doi:10.1002/0471264180.os015.06.
^ Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (1st ed.). Oxford University Press. p. 532. ISBN 978-0-19-850346-0.
^ M. Bolte and M. Scholtyssik (October 1997). "Dimedone at 133K". Acta Crystallogr. C. 53 (10): IUC9700013. doi:10.1107/S0108270197099423.

[1] R. L. Shriner and H. R. Todd (1935). "5,5-dimethyl-1,3-cyclohexanedione". Organic Syntheses. 15: 16. doi:10.1002/0471264180.os015.06.

[2] Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (1st ed.). Oxford University Press. p. 532. ISBN 978-0-19-850346-0.

[3] M. Bolte and M. Scholtyssik (October 1997). "Dimedone at 133K". Acta Crystallogr. C. 53 (10): IUC9700013. doi:10.1107/S0108270197099423.

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