Pyrylium

Pyrylium  |

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Names
Other names

Pyranium

Identifiers

CAS Number

* 289-67-8 Y

3D model (JSmol)

* Interactive image

Beilstein Reference

| 1421881
ChEBI |

* CHEBI:36120 Y
* salt: CHEBI:59658
* family: CHEBI:59657

ChemSpider |

* 7827742 Y

Gmelin Reference

| 558560

PubChem CID

* 9548819

InChI

* InChI=1S/C5H5O/c1-2-4-6-5-3-1/h1-5H/q+1 N

Key: WVIICGIFSIBFOG-UHFFFAOYSA-N N

* InChI=1/C5H5O/c1-2-4-6-5-3-1/h1-5H/q+1

Key: WVIICGIFSIBFOG-UHFFFAOYAF

SMILES

* [o+]1ccccc1

Properties

Chemical formula

| C5H5O+
Molar mass | 81.09 g/mol
Related compounds

Related compounds

| thiopyrylium, selenopyrylium, telluropyrylium

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

N verify (what is YN ?)
Infobox references

Pyrylium is a cation (positive ion) with formula C

5O+
, consisting of a six-membered ring of five carbon atoms, each with one hydrogen atom, and one positively charged oxygen atom. The bonds in the ring are conjugated as in benzene, giving it an aromatic character. In particular, because of the positive charge, the oxygen atom is trivalent. Pyrilium is a mono-cyclic and heterocyclic compound, one of the oxonium ions.

## Contents

* 1 Salts
* 2 Derivatives
* 3 Chemical properties
* 4 Synthesis
* 5 Derivatives
* 6 Pyrones
* 6.1 Chemical properties
* 7 Polycyclic pyrylium ions
* 7.1 Chromenylium ion
* 7.2 Flavylium ion
* 7.3 Naphthoxanthenium cation
* 8 See also
* 9 References

## Salts

Pyrylium and its derivatives form stable salts with a variety of anions.[1][2][3][4][5][6]

## Derivatives

Many important cations are formally derived from pyrylium by substitution of various functional groups for some or all the hydrogens in the ring. The 2,4,6-triphenylpyrilium, referred to as the Katritzky salt, (after Alan R. Katritzky) is an important example used in many modern examples of metal catalyzed cross-couplings.[7]

## Chemical properties

Like other oxonium ions, pyrylium is unstable in neutral water. However, pyrylium is much less reactive than ordinary oxonium ions because of aromatic stabilization. The 2,4,6-triphenyl salt is commonly reacted with aliphatic amines at the 1 position, forming pyridinium salts and activating them towards oxidative addition by metal complexes, most notably ones with nickel.[8] Pyrylium cations also react with nucleophiles in the 2, 4, and 6 positions, which can induce a variety of reactions. The high electronegativity of the oxygen results in strong single perturbation by one heteroatom in the six-membered ring.

## Synthesis

Pyrylium salts are easily produced from simple starting materials through a condensation reaction.

Pyrylium salts with aromatic substituents, such 2,4,6-triphenylpyrylium tetrafluoroborate, can be obtained from two moles of acetophenone and one mole of benzaldehyde in the presence of tetrafluoroboric acid and an oxidizing agent (Dilthey synthesis). For pyrylium salts with alkyl substituents, such as 2,4,6-trimethylpyrylium salts, the best method uses the Balaban-Nenitzescu-Praill synthesis from tertiary butanol and acetic anhydride in the presence of tetrafluoroboric, perchloric, or trifluoromethanesulfonic acids.[9][10] 2,4,6-Triphenylpyrylium salts are converted by bases into a stable 1,5-enedione (pseudobase), but 2,4,6-trimethylpyrylium salts on treatment with hot alkali hydroxides afford an unstable pseudobase that undergoes an intramolecular condensation yielding 3,5-dimethylphenol. In warm deuterium oxide, 2,4,6-trimethylpyrylium salts undergo isotopic exchange of 4-methyl hydrogens faster than for the 2- and 6-methyl groups, allowing the synthesis of regioselectively deuterated compounds.

## Derivatives

The reactivity of pyrylium salts toward nucleophiles makes them useful materials for producing other compounds with stronger aromatic character. Pyrylium salts afford pyridines with ammonia,[11] pyridinium salts with primary amines, pyridine-N-oxides with hydroxylamine, phosphabenzenes with phosphine derivatives, thiopyrylium salts with hydrogen sulfide, and benzene derivatives with acetonitrile or nitromethane.

## Pyrones

A pyrylium cation with a hydroxyl anion substituent in the 2-position is not the zwitterionic aromatic compound (1), but the neutral unsaturated lactone 2-pyrone or pyran-2-one (2). Important representatives of this class are the coumarins. Likewise a 4-hydroxyl pyrylium compound is a γ-pyrone or pyran-4-one (4), to which group belong compounds such as maltol.

### Chemical properties

2-Pyrones are known to react with alkynes in a Diels–Alder reaction to form arene compounds with expulsion of carbon dioxide, for example:[12]

## Polycyclic pyrylium ions

### Chromenylium ion

One bicyclic pyrylium ion is called benzopyrylium ion (IUPAC: chromenylium ion) (formula: C

7O+
, molar mass: 131.15 g/mol, exact mass: 131.04968983). It can be seen as a charged derivative of 2H-1-benzopyran (IUPAC: 2H-chromene, C

8O), or a (charged) substituted heterocyclic derivative of naphthalene (C
10H
8).

### Flavylium ion

In biology, the 2-phenylbenzopyrylium (2-phenylchromenylium) ion is referred to as flavylium. A class of flavylium-derived compounds are anthocyanidins and anthocyanins, pigments that are responsible for the colors of many flowers.[citation needed]

### Naphthoxanthenium cation

Higher polycyclic derivatives of pyrylium also exist. One good example is naphthoxanthenium. This dye is highly stable, aromatic, and planar. It absorbs in the UV and blue region and presents exceptional photophysical properties. It can be synthesized by chemical or photochemical reactions.[13]

* Benzopyrylium chloride (chromenylium chloride), a salt with chloride as the counterion

* Flavylium cation

* Naphthoxanthenium.svg

Naphthoxanthenium cation

## See also

* 6-membered aromatic rings with one carbon replaced by another group: borabenzene, silabenzene, germabenzene, stannabenzene, pyridine, phosphorine, arsabenzene, stibabenzene, bismabenzene, pyrylium, thiopyrylium, selenopyrylium, telluropyrylium
* Pyran, C

6O (pyrones lacking the ketone group)

## References

1. ↑ Gilchrist, T. L. (1997). Heterocyclic Chemistry. ISBN 0-582-27843-0.
2. ↑ Balaban, A. T.; Schroth, W.; Fischer, G. (1969). Pyrylium Salts. I. Synthesis. Advances in Heterocyclic Chemistry. 10. New York: Academic Press. pp. 241–326. doi:10.1016/S0065-2725(08)60499-7.
3. ↑ Balaban, A. T.; Dinculescu, A.; Dorofeenko, G. N.; Fischer, G. W.; Koblik, A. V.; Mezheritskii, V. V.; Schroth, W. (1982). Katritzky, A. R.. ed. Pyrylium Salts. Syntheses, Reactions and Physical Properties. Advances in Heterocyclic Chemistry: Supplement. 2. New York: Academic Press. ISBN 978-0-12-020652-0.
4. ↑ Balaban, A. T. (1979). "The Pyrylium Cation as a Synthon in Organic Chemistry". New Trends in Heterocyclic Chemistry. Studies in Organic Chemistry. 3. Amsterdam: Elsevier. pp. 79–111. ISBN 978-0-444-41737-4. https://archive.org/details/comprehensivecar0000unse/page/79.
5. ↑ Balaban, A. T. (1987). "Pyrylium Salts as Useful Synthons". in Chizov, O.. Organic Synthesis: Modern Trends. Oxford: Blackwell. pp. 263–274. ISBN 0-632-02014-8.
6. ↑ Balaban, T. S.; Balaban, A. T. (2003). "Pyrylium Salts". Hetarenes and Related Ring Systems, Six-membered Hetarenes with one Chalcogen. Science of Synthesis; Houben-Weyl Methods of Molecular Transformations. 14. Stuttgart: Georg Thieme Verlag. pp. 11–200. ISBN 978-3-13-118641-6.
7. ↑ Balaban, A. T.; Wray, V. (1977). "13C n.m.r. spectra of some pyrylium salts and related compounds". Organic Magnetic Resonance 9 (1): 16–22. doi:10.1002/mrc.1270090105.
8. ↑ Pang, Yue; Moser, Daniel; Cornella, Josep (2020). "Pyrylium Salts: Selective Reagents for the Activation of Primary Amino Groups in Organic Synthesis". Synthesis 52 (4): 489–503. doi:10.1055/s-0039-1690703. https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0039-1690703.
9. ↑ Balaban, A. T.; Boulton, A. J. (1973). "2,4,6-Trimethyl-Pyrylium Tetrafluoroborate". Organic Syntheses. http://www.orgsyn.org/orgsyn/pdfs/CV5P1112.pdf. ;  Collective Volume, 5, pp. 1112–1113
10. ↑ Balaban, A. T.; Boulton, A. J. (1973). "2,4,6-Trimethyl-Pyrylium Trifluoromethanesulfonate". Organic Syntheses. http://www.orgsyn.org/orgsyn/pdfs/CV5P1114.pdf. ;  Collective Volume, 5, pp. 1114–1116
11. ↑ Anderson, A. G.; Stang, P. J. (1981). "2,6-Di-tert-Butyl-4-Methylpyridine". Organic Syntheses 60: 34. http://www.orgsyn.org/orgsyn/pdfs/CV7P0144.pdf. ;  Collective Volume, 7, pp. 144
12. ↑ Delaney, P. M.; Moore, J. E.; Harrity, J. P. A. (2006). "An Alkynylboronic Ester Cycloaddition Route to Functionalised Aromatic Boronic Esters". Chemical Communications 2006 (31): 3323–3325. doi:10.1039/b607322k. PMID 16883424.
13. ↑ Bucher, G.; Bresolí-Obach, R.; Brosa, C.; Flors, C.; Luis, J. L.; Grillo, T. A.; Nonell, S. (2014). "β-Phenyl quenching of 9-phenylphenalenones: a novel photocyclisation reaction with biological implications". Physical Chemistry Chemical Physics 16 (35): 18813–18820. doi:10.1039/C4CP02783C. PMID 25079707. Bibcode: 2014PCCP...1618813B.

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