Editing Lactone

{{short description|Cyclic carboxylic ester}}

'''Lactones''' are cyclic [[carboxylic ester]]s. They are derived from the corresponding [[hydroxycarboxylic acid]]s by [[esterification]]. They can be saturated or unsaturated.<ref>{{citation | entry=lactones | title=[[Compendium of Chemical Terminology]] | publisher=[[International Union of Pure and Applied Chemistry]] | version=2.3.3 | date=2014-02-24 | page=817}}</ref>

Lactones are formed by '''lactonization''', the intramolecular esterification of the corresponding hydroxycarboxylic acids.<ref>{{citation | author=Francis A. Carey | author2=Robert M. Giuliano | title=Organic Chemistry | edition=8th | publisher=McGraw-Hill | year=2011 | pages=798–799}}</ref>

==Nomenclature==
[[Greek alphabet#Letters|Greek prefix]]es in alphabetical order indicate ring size.

{| class="wikitable skin-invert"
! Ring size<br />(number of atoms<br/> in the ring)
! {{nobr|[[Systematic name]]}}
! [[IUPAC name]]
! Parent lactone
! Structure, comment
|-
|3
|[[α-lactone]]
|Oxiran-2-one
|[[Acetolactone]]
|[[File:Acetolactone-2D-skeletal.png|left|frameless|120x120px]]
|-
|4
|[[β-lactone]]
|Oxetan-2-one
|{{ubl|β-Propiolactone|Propiolactone}}
|[[File:Propiolactone.png|100px]]

|-
|5
|[[γ-lactone]]
|Oxolan-2-one
|γ-Butyrolactone
|[[File:GBL chemical structure.svg|100px]]

|-
|6
|[[δ-lactone]]
|Oxan-2-one
|{{ubl|[[δ-Valerolactone]]}}
|[[file:delta-valerolactone.png|100px]]
|-
|7
|[[ε-lactone]]
|Oxepan-2-one
|{{ubl|ε-Caprolactone|Caprolactone|Hexanolide}}
|[[File:Caprolactone.png|85px]]
|}

Lactones are usually named according to the precursor acid molecule (''aceto'' = 2 carbon atoms, ''propio'' = 3, ''butyro'' = 4, ''valero'' = 5, ''capro'' = 6, etc.), with a ''-lactone'' suffix and a Greek letter prefix that specifies the number of carbon atoms in the heterocycle — that is, the distance between the relevant -OH and the -COOH groups along said backbone. The first carbon atom after the carbon in the -COOH group on the parent compound is labelled α, the second will be labeled β, and so forth. Therefore, the prefixes also indicate the size of the lactone ring: α-lactone = 3-membered ring, β-lactone = 4-membered, γ-lactone = 5-membered, δ-lactone = 6-membered, etc. {{anchor|macrolactone}}[[Macrocyclic]] lactones are known as '''macrolactones'''.<ref>{{cite web|url=http://www.chem.ucla.edu/~harding/IGOC/M/macrolactone.html|title=Illustrated Glossary of Organic Chemistry|author=Steven A. Hardinger|publisher=Department of Chemistry & Biochemistry, [[University of California, Los Angeles|UCLA]]}}</ref>{{wiktionary|macrolactone}}

The other suffix used to denote a lactone is ''-olide'', used in substance class names like ''[[butenolide]]'', ''[[macrolide]]'', ''[[cardenolide]]'' or ''[[bufadienolide]]''.

To obtain the [[preferred IUPAC name]]s, lactones are named as heterocyclic pseudoketones by adding the suffix 'one', 'dione', 'thione', etc. and the appropriate multiplicative prefixes to the name of the heterocyclic parent hydride.<ref>{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = [[Royal Society of Chemistry|The Royal Society of Chemistry]] | date = 2014 | location = Cambridge | page = 822 | doi = 10.1039/9781849733069-00648 | isbn = 978-0-85404-182-4}}</ref>

==Etymology==
The name ''lactone'' derives from the ring compound called [[lactide]], which is formed from the dehydration of 2-hydroxypropanoic acid ([[lactic acid]]) CH<sub>3</sub>-CH(OH)-COOH. Lactic acid, in turn, derives its name from its original isolation from soured milk (Latin: lac, lactis). The name was coined in 1844 by the French chemist [[Théophile-Jules Pelouze]], who first obtained it as a derivative of lactic acid.<ref>{{cite journal |last1=Pelouze |first1=J. |title=Mémoire sur l'acide lactique |journal=Comptes rendus |date=9 December 1844 |volume=19 |pages=1219–1227 |url=https://www.biodiversitylibrary.org/item/81358#page/1237/mode/1up |trans-title=Memoir on lactic acid |language=fr}}
From p. 1223:  ''"Indépendamment de la lactide dont je viens de rappeler l'existence dans les produits de la distllation de l'acide lactique, celui-ci donne encore, par sa décomposition, une autre substance, que je propose d'appeler ''lactone'', parce qu'elle me paraît être à l'acide lactique ce que l'acétone est à l'acide acétique."''  (Independently of the lactide of which I have just recalled the existence in the products of the distillation of lactic acid, this [i.e., lactic acid] gives further, by its decomposition, another substance, which I propose to call ''lactone'', because it seems to me to be to lactic acid what acetone is to acetic acid.)
*  Reprinted:  {{cite journal |last1=Pelouze |first1=J. |title=Mémoire sur l'acide lactique |journal=Annales de Chimie et de Physique |date=1845 |volume=13 |pages=257–268 |url=https://babel.hathitrust.org/cgi/pt?id=hvd.hx3dxr&view=1up&seq=276&q1=262 |series=3rd series |trans-title=Memoir on lactic acid |language=fr}} ; see p. 262.
*  English translation:  {{cite journal |last1=Pelouze |first1=J. |title=Researches on lactic acid |journal=The Chemical Gazette |date=January 15, 1845 |volume=3 |issue=54 |pages=29–35 |url=https://books.google.com/books?id=1BkFAAAAQAAJ&pg=PA29}} ; see p. 31.
*  {{cite book |last1=Menten |first1=Pierre de |title=Dictionnaire de chimie: Une approche étymologique et historique |trans-title=Dictionary of Chemistry: an etymological and historical approach |date=2013 |publisher=de boeck |location=Brussels, Belgium |page=183 |isbn=9782804181758 |url=https://books.google.com/books?id=NKTKDgAAQBAJ&pg=PA183 |language=fr}}</ref> An internal [[dehydration reaction]] within the same molecule of lactic acid would have produced [[alpha-propiolactone]], a lactone with a 3-membered ring.

In 1880 the German chemist [[Wilhelm Rudolph Fittig]] extended the name "lactone" to all intramolecular carboxylic esters.<ref>{{cite journal |last1=Fittig |first1=Rudolph |title=Untersuchungen über ungesättige Säuren, dritte Abhandlung |journal=Annalen der Chemie und Pharmacie |date=1880 |volume=200 |pages=1–96 |doi=10.1002/jlac.18802000102 |url=https://babel.hathitrust.org/cgi/pt?id=uiug.30112025844553&view=1up&seq=72 |trans-title=Investigations into unsaturated acids, third article |language=de}}  From p. 62:  ''"Es ist wünschenswerth, für diese Gruppe von Verbindungen, deren bis jetzt einfachster Repräsentant der im Vorstehenden beschriebene Körper ist, eine allgemeine Bezeichnungsweise zu haben, und da der Name "Lactide" nicht anwendbar ist, weil dann das Lactid κατ εξοχην kein Lactid sein wurde, so schlagen wir als Gruppenbezeichnung den Namen "Lactone" vor".'' (It's desirable for this group of compounds — whose simplest representative until now has been the substance that's described in the preceding — to have a general designation, and since the name "lactide" isn't applicable because then the archetypal lactide would not be a lactide, we therefore suggest the name "lactone" as the designation of this group [of compounds].)</ref>

== Occurrence ==
[[File:Glucono-delta-lactone-2D-skeletal.png|right|thumb|110px|[[glucono delta-lactone|<small>D</small>-glucono-δ-lactone]] ([[E number|E575]])]]
Lactone rings occur widely as building blocks in nature, such as in [[ascorbic acid]], [[kavain]], [[nepetalactone]], [[gluconolactone]], [[hormones]] ([[spironolactone]], [[mevalonolactone]]), [[enzymes]] ([[lactonase]]), [[neurotransmitter]]s ([[butyrolactone]], [[avermectin]]s), [[antibiotic]]s ([[macrolide]]s like [[erythromycin]]; [[amphotericin B]]), [[anticancer drugs]] ([[vernolepin]], [[epothilones]]), [[phytoestrogen]]s ([[resorcylic acid]] lactones, [[cardiac glycoside]]s).

5-Membered γ-lactones and 6-membered δ-lactones are prevalent. β-lactones appear in a number of natural products.<ref name=DNThiolSynth>{{cite journal|doi=10.1021/jo00003a047|pages=1176–1185|journal=Journal of Organic Chemistry|year=1991|volume=56|title=A practical and efficient method for the synthesis of β{{nbh}}lactones|first1=Rick&nbsp;L.|last1=Danheiser|first2=James&nbsp;S.|last2=Nowick|orig-date=25 July 1990|number=3}}</ref>  α{{nbh}}Lactones can be detected as transient species in [[mass spectrometry]] experiments.<ref>Detlef Schröder, Norman Goldberg, Waltraud Zummack, [[Helmut Schwarz]], John C. Poutsma and Robert R. Squires (1997), ''Generation of α-acetolactone and the acetoxyl diradical •CH2COO• in the gas phase''. International Journal of Mass Spectrometry and Ion Processes, Volumes 165-166, November issue, Pages 71-82. {{doi|10.1016/S0168-1176(97)00150-X}}</ref> 

Macrocyclic lactones are also important natural products.<ref name="fnf">{{citation | author=Karl-Georg Fahlbusch | contribution=Flavors and Fragrances | title=[[Ullmann's Encyclopedia of Industrial Chemistry]] | edition=7th | publisher=Wiley | year=2007 | pages=74‒78|display-authors=etal}}</ref> Lactones are present in [[oak]] wood, and they contribute to the flavour profile of [[barrel-aged beer]]s.<ref>{{cite web|url=https://beerandbrewing.com/dictionary/h63PzW6oDQ/ |website=Craft Beer and Brewing|title=The Oxford Companion to Beer definition of barrel-aging|first = Garrett|last = Oliver}}</ref>

==Synthesis==
[[File:Oxandrolones synthesis.svg|thumb|right|Oxandrolone synthesis]]

Many methods in ester synthesis can also be applied to that of lactones. Lactonization competes with [[polymerization]] for longer hydroxy acids, or the strained β{{nbh}}lactones. γ{{nbh}}Lactones, on the other hand, are so stable that 4-hydroxy acids (R-CH(OH)-(CH<sub>2</sub>)<sub>2</sub>-CO<sub>2</sub>H) spontaneously cyclize.

In one industrial synthesis of [[oxandrolone]] the key lactone-forming step is an [[organic reaction]] – esterification.<ref>''Development of a Commercial Process to Produce Oxandrolone'' John E. Cabaj, David Kairys, and Thomas R. Benson Org. Process Res. Dev.; '''2007'''; 11(3) pp 378–388; (Article) {{doi|10.1021/op060231b}}</ref><ref>The complete reaction sequence is [[bromination]] to a [[haloketone]] (not displayed), [[elimination reaction]] with [[lithium chloride]] to an [[enone]], [[organic oxidation]] by [[osmium tetroxide]] and [[lead tetraacetate]] with ring-opening and finally reduction of the [[aldehyde]] to the [[Alcohol (chemistry)|alcohol]] with [[sodium borohydride]] and intramolecular lactone formation</ref>

[[File:Iodolactonization.svg|thumb|right|iodolactonization]]
In [[halolactonization]], an [[alkene]] is attacked by a [[halogen]] via [[electrophilic addition]] with the cationic intermediate captured intramolecularly by an adjacent [[carboxylic acid]].<ref>[[Organic Syntheses]], Coll. Vol. 7, p.164 (1990); Vol. 64, p.175 ('''1986''') [http://orgsynth.org/orgsyn/pdfs/CV7P0164.pdf Article link]</ref>

Specific methods include [[Yamaguchi esterification]], [[Shiina macrolactonization]], [[Corey-Nicolaou macrolactonization]], [[Baeyer–Villiger oxidation]] and [[nucleophilic abstraction]].

[[File:γ-Lactones synthesis.svg|thumb|right|γ-Lactone synthesis from fatty alcohols and acrylic acid]]

An alternative radical reaction yielding γ-lactones is the [[manganese-mediated coupling reactions|manganese-mediated coupling]].

==Reactions==
Lactones exhibit the reactions characteristic of esters.

===Hydrolysis and aminolysis===
Heating a lactone with a base ([[sodium hydroxide]]) will [[hydrolyse]] the lactone to its parent compound, the straight chained bifunctional compound. Like straight-chained esters, the hydrolysis-condensation reaction of lactones is a [[reversible reaction]], with an [[chemical equilibrium|equilibrium]]. However, the [[equilibrium constant]] of the hydrolysis reaction of the lactone is lower than that of the straight-chained ester i.e. the products (hydroxyacids) are less favored in the case of the lactones. This is because although the [[enthalpy|enthalpies]] of the hydrolysis of esters and lactones are about the same, the [[entropy]] of the hydrolysis of lactones is less than the entropy of straight-chained esters. Straight-chained esters give two products upon hydrolysis, making the entropy change more favorable than in the case of lactones which gives only a single product.

Lactones also react with amines to give the ring-opened alcohol and amide.

===Reduction===
Lactones can be reduced to diols using [[lithium aluminium hydride]]. For instance, gamma-lactones is reduced to butane-1,4-diol, (CH<sub>2</sub>(OH)-(CH<sub>2</sub>)<sub>2</sub>-CH<sub>2</sub>(OH).

=== Polymerization ===
Some lactones convert to polyesters:<ref>{{citation | author=Wilhelm Riemenschneider | author2=Hermann M. Bolt | contribution=Esters, Organic | title=[[Ullmann's Encyclopedia of Industrial Chemistry]] | edition=7th | publisher=Wiley | year=2007}}</ref><ref>{{Cite journal|last1=Chandru|first1=Kuhan|last2=Jia|first2=Tony Z.|last3=Mamajanov|first3=Irena|last4=Bapat|first4=Niraja|last5=Cleaves|first5=H. James|date=2020-10-16|title=Prebiotic oligomerization and self-assembly of structurally diverse xenobiological monomers|url= |journal=Scientific Reports|language=en|volume=10|issue=1|pages=17560|doi=10.1038/s41598-020-74223-5|issn=2045-2322|pmc=7567815|pmid=33067516|bibcode=2020NatSR..1017560C}}</ref> For example the double lactone called [[lactide]] polymerizes to [[polylactic acid]] (polylactide). The resulting polylactic acid has been heavily investigated for commercial applications.<ref>{{cite book | isbn = 978-0-470-29366-9 | title = Poly(lactic acid): Synthesis, Structures, Properties, Processing, and Applications | author1 = R. Auras | author2 = L.-T. Lim | author3= S. E. M. Selke |author4= H. Tsuji | publisher = Wiley | year = 2010 }}</ref><ref>{{cite journal|title=Controlled Ring-Opening Polymerization of Lactide and Glycolide|author1=Odile Dechy-Cabaret |author2=Blanca Martin-Vaca |author3=Didier Bourissou | journal=Chem. Rev.|year=2004|volume=104|issue=12|pages=6147–76|doi=10.1021/cr040002s|pmid=15584698}}</ref>

:[[File:Polylactide_synthesis_v.1.png|400px|class=skin-invert]]

== Uses ==

=== Flavors and fragrances ===
Lactones contribute significantly to the flavor of fruit, and of unfermented and fermented dairy products,<ref name=Berger07>{{cite book|editor1-last=Berger|editor1-first=R.G.|title=Flavours and fragrances chemistry, bioprocessing and sustainability|date=2007|publisher=Springer|location=Berlin|isbn=9783540493396|url=https://books.google.com/books?id=ax1OvyH8jGoC&pg=PA557|access-date=2 July 2015}}</ref> and are therefore used as flavors and fragrances.<ref name="fnf" /> Some examples are [[γ-decalactone]] (4-decanolide), which has a characteristic peach flavor;<ref name="Berger07" /> [[δ-decalactone]] (5-decanolide), which has a creamy coconut/peach flavour; γ-dodecalactone (4-dodecanolide), which also has a coconut/fruity flavor,<ref name="Berger07" /> a description which also fits [[γ-octalactone]] (4-octanolide),<ref>{{cite book|editor1-last=Mehta|editor1-first=Bhavbhuti M.|editor2-last=Kamal-Eldin|editor2-first=Afaf|editor3-last=Iwanski|editor3-first=Robert Z.|title=Fermentation effects on food properties|date=2012|publisher=Taylor & Francis|location=Boca Raton|isbn=9781439853351|page=74|url=https://books.google.com/books?id=QanMBQAAQBAJ&pg=PA74|access-date=2 July 2015}}</ref> although it also has a herbaceous character;<ref name="Berger07" /> [[γ-nonalactone]], which has an intense coconut flavor of this series, despite not occurring in coconut,<ref>{{cite book|editor1-last=Marsili|editor1-first=Ray|title=Sensory-directed flavor analysis|date=2007|publisher=CRC/Taylor & Francis|location=Boca Raton, FL|isbn=9781420017045|page=242|url=https://books.google.com/books?id=tJ0JLpA5Mc0C&pg=PA242|access-date=2 July 2015}}</ref> and [[Γ-lactone|γ-undecalactone]].

Macrocyclic lactones ([[cyclopentadecanolide]], [[15-pentadec-11/12-enolide]]) have odors similar to macrocyclic ketones of animal origin ([[muscone]], [[civetone]]).<ref name="fnf" />

=== Plastics ===
[[Polycaprolactone]] is an important plastic. Its formation has even been considered in the context of the [[Abiogenesis|origin of life]].<ref>{{Cite journal|last1=Chandru|first1=Kuhan|last2=Mamajanov|first2=Irena|last3=Cleaves|first3=H. James|last4=Jia|first4=Tony Z.|date=January 2020|title=Polyesters as a Model System for Building Primitive Biologies from Non-Biological Prebiotic Chemistry|journal=Life|language=en|volume=10|issue=1|pages=6|doi=10.3390/life10010006|pmc=7175156|pmid=31963928|bibcode=2020Life...10....6C |doi-access=free}}</ref>

== Dilactones ==
*[[Ellagic acid]] (Hexahydroxydiphenic acid dilactone)
*[[Flavogallonic acid dilactone]] can be found in ''[[Rhynchosia volubilis]]'' seeds and in ''Shorea laeviforia''
*[[Lactide]]
*[[Tergallic acid dilactone]] can be found in ''Rhynchosia volubilis'' seeds
*[[Valoneic acid dilactone]] can be isolated from the heartwood of ''Shorea laeviforia''
*[[Ethylene brassylate]] (Musk T), a widely used synthetic musk

== See also ==
{{wiktionary}}
* [[Lactam]], a cyclic [[amide]]
* [[Lactim]], a cyclic [[imide]]
* [[Lactide]], a cyclic di[[ester]]
* [[Halolactonization]]
* [[Phthalein]]
* [[Ester]] 

==References and notes==
{{reflist}}

{{Authority control}}

[[Category:Lactones| ]]
[[Category:Functional groups]]