Zincke reaction

Reaction mechanism

The first reaction is the formation of the N-2,4-dinitrophenyl-pyridinium salt (2). This salt is typically isolated and purified by recrystallization.

Upon heating a primary amine with the N-2,4-dinitrophenyl-pyridinium salt (2), the addition of the amine leads to the opening of the pyridinium ring. A second addition of amine leads to the displacement of 2,4-dinitroaniline (5) and formation of the König salt{{cite journal

This mechanism can be referred to as an instance of the ANRORC mechanism: nucleophilic addition (AN), ring opening and ring closing.

Applications

In one solid-phase synthesis application, the amine is covalently attached to Wang resin.

Another example is the synthesis of a chiral isoquinolinium salt.

Zincke aldehydes

Main article: Zincke aldehyde

With secondary amines and not primary amines the Zincke reaction takes on a different shape forming so-called Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde:

This variation has been applied in the synthesis of novel indoles:

with cyanogen bromide mediated pyridine activation.

2007 rediscovery

In 2006 and again in 2007 the Zincke reaction was rediscovered by a research group from Japan and a group from the USA. Both groups claimed the synthesis of a 12 membered diazaannulene (structure 1) from an N-aryl pyridinium chloride and an amine, an aniline in the case of the Japanese group (depicted below) and an aliphatic amine (anticipating surfactant properties) in the case of the American group.

:[[Image:DiazaAnnulene.svg|600px|alleged diaza annulene synthesis Yamaguchi 2007]]

In a letter to Angewandte Chemie, the German chemist Manfred Christl pointed out not only that the alleged new chemistry was in fact 100-year-old Zincke chemistry but also that the proposed structure for the reaction product was not the 12 membered ring but the 6 membered pyridinium salt (structure 2). Initially both groups conceded that they had ignored existing literature on Zincke but held on to the annulene structure based on their electrospray ionization (ESI) results which according to them clearly showed dimer. In his letter Christl remarked that in ESI measurements association of molecules is a common phenomenon. In addition, he noted similarities in melting point and NMR spectroscopy.

As of December 2007 the Japanese group retracted its paper in Organic Letters due to uncertainties regarding what products are formed in the reaction described and the US group added a correction to theirs in the Angewandte Chemie stating they wish(ed) to alter the proposed structure of (the) annulene. The issue did receive some media coverage:

References

References

1. (1970). "Formation of phenylpyridinium chloride from 5-anilino-N-phenyl-2,4-pentadienylideniminium chloride. Kinetics in basic media". Journal of the American Chemical Society.
2. (1970). "Influence of para substituents on the rate of cyclization of 5-anilino-N-phenyl-2,4-pentadienylidenimine". Journal of the American Chemical Society.
3. (2000). "The Solid-Phase Zincke Reaction: Preparation of ω-Hydroxy Pyridinium Salts in the Search for CFTR Activation". The Journal of Organic Chemistry.
4. (1996). "New Chiral Isoquinolinium Salt Derivatives from Chiral Primary Amines ''via '' Zincke Reaction". The Journal of Organic Chemistry.
5. (2006). "Synthesis of Nitrogen Heterocycles by the Ring Opening of Pyridinium Salts". Angewandte Chemie International Edition.
6. (2006). "One-Pot Synthesis of ''N'' -Substituted Diaza[12]annulenes". Organic Letters.
7. (2007). "[12]Annulene Gemini Surfactants: Structure and Self-Assembly". Angewandte Chemie International Edition.
8. (2007). "1,7-Diaza[12]annulene Derivatives? 100-Year-Old Pyridinium Salts!". Angewandte Chemie International Edition.
9. (2007). "[12]Annulene Gemini Surfactants: Structure and Self-Assembly". Angewandte Chemie International Edition.
10. {{in lang. de ''Ahnungslose Chemiker entdecken Verbindung zum zweiten Mal.'' Jens Lubbadeh [[Der Spiegel]] 6 December '''2007''' http://www.spiegel.de/wissenschaft/natur/0,1518,521646,00.html
11. Sanderson, Katharine. (4 December 2007). "Where have I seen that before? 103-year-old chemical reaction pops up again". [[Nature (journal).