Chemistry:Triacetic acid lactone
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| Preferred IUPAC name
4-Hydroxy-6-methyl-2H-pyran-2-one | |
Other names
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3D model (JSmol)
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PubChem CID
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| Properties | |
| C6H6O3 | |
| Molar mass | 126.12 g mol−1 |
| Appearance | light yellow crystal powder |
| Density | 1.348 g cm−3 |
| Melting point | 188 to 190 °C (370 to 374 °F; 461 to 463 K) |
| Boiling point | 285.9 °C (546.6 °F; 559.0 K) |
| 8.60 g L-1 at 20°C in H2O | |
| Hazards | |
| Main hazards | Moderately Toxic |
| GHS pictograms | 
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| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
| Flash point | 127.9 °C (262.2 °F; 401.0 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Triacetic acid lactone (TAL;[1] 4-hydroxy-6-methyl-2-pyrone) is an organic compound derived enzymatically from glucose. It is a light yellow solid that is soluble in organic solvents.
Structure
Triacetic acid lactone consists of two main tautomers.
The tautomer on the left, featuring a 4-hydroxy group, the C4 carbon, is dominant. Triacetic acid lactone is classified as a 2-pyrone compound owing to the ketone group on the C2 carbon in its dominant form.
Synthesis
Triacetic acid lactone is synthesized either from dehydroacetic acid, another 2-pyrone derivative, or from glucose by enzymatic catalysis. In its original synthesis, triacetic acid lactone was obtained by treatment of dehydroacetic acid with sulfuric acid at 135 °C. Dehydroacetic acid undergoes ring-opening and hydration to form "tetracetic acid".[2] Upon cooling, triacetic acid reverts to a lactone ring similar to the dehydroacetic acid structure, and the triacetic acid lactone is recovered by crystallization in cold water.
Biosynthesis
The microbial synthesis of triacetic acid lactone requires the enzyme 2-pyrone synthase (2-PS).[3] This enzyme has been examined in two hosts Escherichia coli and Saccharomyces cerevisiae. The Saccharomyces cerevisiae host being used during the synthesis produces a higher yield (70%) compared with the Escherichia coli host, which produces a yield of 40% of triacetic acid lactone. This enzyme catalyzes the synthesis of triacetic acid lactone from acetyl-CoA via two subsequent condensations with malonyl-CoA. This produces an intermediate of 3,5-diketohexanoate thioester, which undergoes ring closure to produce triacetic acid lactone.
Reactivity
The lactone is a versatile intermediate in organic synthesis. Substantial negative charge accumulates on the C3 carbon, rendering it nucleophilic, but the C5 carbon is inert. [4]
It has also been described as a platform chemical, meaning that it could be the precursor to other fine chemicals. The lactone undergoes decarboxylation to acetylacetone. It is also a precursor to sorbic acid, dienoic acid, and hexenoic acid. Dienoic acid is used to inhibit the growth of various molds and hexenoic acid is used as a flavoring agent.[5] Acetylacetone is used for metal extraction and plating and as a food additive.[6]
See also
- 4-Hydroxycoumarin - bicyclic analogue
References
- ↑ "New Sustainable Production Method Could Advance Plastics and Pharmaceuticals" (Press release). University of Texas. 13 February 2018 – via Drug Discovery & Development Magazine.
- ↑ Collie, J. Norman (1891). "LVI.?The lactone of triacetic acid". Journal of the Chemical Society, Transactions 59: 607–617. doi:10.1039/CT8915900607. https://zenodo.org/record/2014590.
- ↑ Xie, Dongming; Shao, Zengyi; Achkar, Jihane; Zha, Wenjuan; Frost, John W.; Zhao, Huimin (2006). "Microbial synthesis of triacetic acid lactone". Biotechnology and Bioengineering 93 (4): 727–36. doi:10.1002/bit.20759. PMID 16245348.
- ↑ Moreno-Mañas, Marcial; Pleixats, Roser (1992). "Dehydroacetic Acid, Triacetic Acid Lactone, and Related Pyrones". Advances in Heterocyclic Chemistry 53: 1–84. doi:10.1016/S0065-2725(08)60861-2. ISBN 9780120207534.
- ↑ Jacoby, Mitch (2012). "Teaming Up for Biobased Chemicals". Chem. Eng. News 90 (32): 37–38. doi:10.1021/cen-09032-scitech1.
- ↑ Chia, Mei; Schwartz, Thomas J.; Shanks, Brent H.; Dumesic, James A. (2012). "Triacetic acid lactone as a potential biorenewable platform chemical". Green Chemistry 14 (7): 1850. doi:10.1039/C2GC35343A.
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