In organic chemistry, a hemiacetal is a functional group the general formula R1R2C(OH)OR, where R1, R2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group) to an aldehyde (R−CH=O) or a ketone (R2C=O) under acidic conditions. The addition of an alcohol to a ketone is more commonly referred to as a hemiketal. Common examples of hemiacetals include cyclic monosaccharides. Hemiacetals have use as a protecting group and in synthesizing oxygenated heterocycles like tetrahydrofurans.
Nomenclature
editAccording to the IUPAC definition of a hemiacetal, the R1 and R2 groups may or may not be hydrogen. In a hemiketal, both of these R-groups must not be hydrogen. Thus, hemiketals are regarded as a subclass of hemiacetals.[1] The prefix hemi, meaning half, refers to the one alcohol added to the carbonyl group. This is half of the required alcohols to form acetals or ketals.[2] Cyclic hemiacetals can sometimes be referred to as lactols.[3]
Formation
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Hemiacetals form in the reaction between alcohols and aldehydes or ketones. Using an acid catalyst, the reaction proceeds via nucleophilic attack of the carbonyl group by the alcohol.[4] A subsequent nucleophilic attack of the hemiacetal by the alcohol results in an acetal.[2] Solutions of simple aldehydes in alcohols mainly consist of the hemiacetal. The equilibrium is dynamic and can be easily reversed via hydrolysis. The equilibrium is sensitive to steric effects.[5]
| Carbonyl compound | alcohol solvent | %hemiacetal |
|---|---|---|
| acetaldehyde | methanol | 97 |
| acetaldehyde | ethanol | 91 |
| propionaldehyde | methanol | 95 |
| bromoacetone | methanol | 47 |
Cyclic hemiacetals often form readily, especially when they are 5- and 6-membered rings. In this case, a hydroxy group reacts with a carbonyl group within the same molecule to undergo an intramolecular cyclization reaction.[6]
Hemiacetals in nature
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Hemiacetals commonly exist in nature as aldoses such as glucose, and hemiketals commonly exist in nature as ketoses such as fructose. The favorability of the formation of a strain-free six-membered ring and the electrophilicity of an aldehyde combine to strongly favor the acetal form.[8]
Usage
editHemiacetals can be strategically used as a protecting group for carbonyls in organic synthesis to prevent unwanted reactions from occurring.[6] A carbonyl can be converted to its hemiacetal form to decrease its reactivity. The desired reaction with the target functional group can then be carried out, and the hemiacetal can later be converted back to a carbonyl via hydrolysis.
Tetrahydrofurans can be synthesized from nucleophilic addition to hemiacetals with high stereoselectivity, which can be further used to form polymers such as lignans.[9]
Hemiacetals can also undergo acid-catalyzed spirocyclization or metal-catalyzed addition/elimination to afford spiroacetals. These reactions are moderately stereoselective, although the thermodynamically-favoured isomer is often produced.[10] Drug discovery programs synthesize spiroacetal scaffolds to generate libraries of spiroacetal-containing molecules. These spiroacetal derivatives have potential use in treating diseases such as CLL leukemia.[11]
One method of producing linear hemiacetal esters is through the condensation of stabilized hemiacetals by anhydrides; this creates a stable hemiketal intermediate that subsequently undergoes acetylation into the hemiacetal ester. Hemiacetal esters are primarily used in polymer chemistry as a polymerization initiator and as a protecting group for carboxylic acids.[12]
References
edit- ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "hemiketals". doi:10.1351/goldbook.H02776
- ^ a b Fox, Marye Anne; Whitesell, James K. (2004). Organic Chemistry. Jones & Bartlett Learning. p. 590. ISBN 9780763721978.
- ^ IUPAC Gold Book lactols
- ^ Azofra, Luis Miguel; Alkorta, Ibon; Elguero, José; Toro-Labbé, Alejandro (2012-08-09). "Mechanisms of Formation of Hemiacetals: Intrinsic Reactivity Analysis". The Journal of Physical Chemistry A. 116 (31): 8250–8259. doi:10.1021/jp304495f. hdl:10553/74807. ISSN 1089-5639.
- ^ a b Schmitz, Ernst; Eichhorn, Inge (1967). "Acetals and Hemiacetals". The Ether Linkage (PATAI'S Chemistry of Functional Groups). pp. 309–351. doi:10.1002/9780470771075.ch7. ISBN 9780470771075.
- ^ a b Solomons, Thomas W. Graham; Fryhle, Craig B.; Snyder, Scott A. (2016). Solomons' organic chemistry (12th, global ed.). Hoboken, New Jersey: John Wiley & Sons, Inc. ISBN 978-1-119-24897-2.
- ^ Salaun, Jacques (1983). "Cyclopropanone Hemiacetals". Chemical Reviews. 83 (6): 619–632. doi:10.1021/cr00058a002.
- ^ "10.3: Hemiacetals, Hemiketals, and Hydrates". Chemistry LibreTexts. 2018-08-10. Retrieved 2024-11-30.
- ^ Rainier, Jon D. (2014), Cossy, Janine (ed.), "Synthesis of Substituted Tetrahydrofurans", Synthesis of Saturated Oxygenated Heterocycles I, vol. 35, Berlin, Heidelberg: Springer Berlin Heidelberg, pp. 1–41, doi:10.1007/978-3-642-41473-2_1, ISBN 978-3-642-41472-5, retrieved 2024-11-30
- ^ Brimble, Margaret A.; Stubbing, Louise A. (2014), Cossy, Janine (ed.), "Synthesis of 5,6- and 6,6-Spirocyclic Compounds", Synthesis of Saturated Oxygenated Heterocycles I, vol. 35, Berlin, Heidelberg: Springer Berlin Heidelberg, pp. 189–267, doi:10.1007/978-3-642-41473-2_5, ISBN 978-3-642-41472-5, retrieved 2024-11-30
- ^ Lenci, Elena (2020-01-01), Trabocchi, Andrea; Lenci, Elena (eds.), "Chapter 8 - Synthesis and biological properties of spiroacetal-containing small molecules", Small Molecule Drug Discovery, Elsevier, pp. 225–245, doi:10.1016/b978-0-12-818349-6.00008-x, ISBN 978-0-12-818349-6
- ^ Boucher, David; Laviéville, Sidonie; Ladmiral, Vincent; Negrell, Claire; Leclerc, Eric (2024-02-13). "Hemiacetal Esters: Synthesis, Properties, and Applications of a Versatile Functional Group". Macromolecules. 57 (3): 810–829. doi:10.1021/acs.macromol.3c01250. ISSN 0024-9297.