Diketone
Diacetyl, the simplest diketone
A diketone or dione is a molecule containing two ketone groups. The simplest diketone is diacetyl, also known as 2,3-butanedione. Diacetyl, acetylacetone, and hexane-2,5-dione are examples of 1,2-, 1,3-, and 1,4-diketones, respectively. Dimedone is an example of a cyclic diketone.
Contents
1 1,2-Diketones
2 1,3-Diketones
3 1,4-Diketones
4 Other diketones
5 EU Regulation
6 See also
7 References
1,2-Diketones
An important member is biacetyl, CH3C(O)C(O)CH3. These compounds are often generated by dehydrogenation of the diols:[1]
- RCH(OH)CH(OH)R → RC(O)C(O)R + 2 H2
A distinctive feature of 1,2-diketones is the long C-C bond linking the carbonyl groups. This bond distance is about 1.54 Å, compared to 1.45 Å for the corresponding bond in 1,3-butadiene. The effect is attributed to repulsion between the partial positive charges of the carbonyl carbon atoms.[2]
1,2-Diketones condense with many bifunctional nucleophiles, such as urea and thiourea to give heterocycles. Upon condensation with aromatic amines, they convert to the diketimine ligands.
1,3-Diketones
An important member is acetylacetone, CH3C(O)CH2C(O)CH3. Acetylacetone is prepared industrially by the thermal rearrangement of isopropenylacetate.[1]
- CH2(CH3)COC(O)Me → MeC(O)CH2C(O)Me
Classically, 1,3-diketones are prepared by condensation of ketones with esters.
1,3-Diketones usually exist predominantly as enols because of conjugation of the enol or enolate with the other carbonyl group, and the stability gained in forming a six-membered ring containing a hydrogen bond. The percent enol in acetylacetone, trifluoroacetyacetone, and hexafluoroacetylacetone are 85, 97, and 100%, respectively (neat, 33 °C).[3]
Like other diketones, 1,3-diketones are versatile precursors to heterocycles. Hydrazine, for example, condenses to give pyrazoles.
The conjugate base derived from 1,3-ketones form coordination complexes. In the DeMayo reaction 1,3-diketones react with alkenes in a photochemical pericyclic reaction to form (substituted) 1,5-diketones.
1,4-Diketones
Diketones with two methylene groups separating the carbonyl groups typically coexist with their enol tautomers. 1,4-Diketones are useful precursors to heterocycles via the Paal-Knorr Synthesis, which gives furans, pyrroles, and thiophenes.
The condensation of 1,4-diketones (and related substrates) with hydrazines afford dihydropyridazines, which can be converted to pyridazines.
Other diketones
The reactions of diketones where the carbonyl centers are separated by three or more methylene groups are similar to those of simple ketones. These longer diketones are generally prone to intramolecular aldol condensations.
EU Regulation
In 2004, the EU conducted an examination of certain flavoring additives grouped together as "Flavouring Group Evaluation FGE.11". This group included diketones.[4] As part of that study, the EU found that acetylacetone (pentane-2,4-dione) (FL 07.191) was genotoxic in vivo and in vitro, and deleted it from the register of permitted flavoring substances.[5] The register of permitted flavoring substances was adopted in 1999.[6]
See also
- Triketone
References
^ ab Hardo Siegel, Manfred Eggersdorfer "Ketones" in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, 2002, Wienheim. doi:10.1002/14356007.a15_077
^ Eriks, K.; Hayden, T. D.; Yang, S. Hsi; Chan, I. Y. (1983). "Crystal and molecular structure of biacetyl (2,3-butanedione), (H3CCO)2, at -12 and -100 °C". J. Am. Chem. Soc. 105 (12): 3940–3942. doi:10.1021/ja00350a032..mw-parser-output cite.citationfont-style:inherit.mw-parser-output .citation qquotes:"""""""'""'".mw-parser-output .citation .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-ws-icon abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center.mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-maintdisplay:none;color:#33aa33;margin-left:0.3em.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em
^ Jane L. Burdett; Max T. Rogers (1964). "Keto-Enol Tautomerism in β-Dicarbonyls Studied by Nuclear Magnetic Resonance Spectroscopy. I. Proton Chemical Shifts and Equilibrium Constants of Pure Compounds". J. Am. Chem. Soc. 86: 2105–2109. doi:10.1021/ja01065a003.
^ Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food, EFSA Journal (2004) 166, 1-44
^ COMMISSION DECISION of 18 May 2005 amending Decision 1999/217/EC as regards the register of flavouring substances used in or on foodstuffs, Official Journal of the European Union
^ Official Journal of the European Communities Archived 2007-11-19 at the Wayback Machine
