Reimer–Tiemann reaction

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Reimer Tiemann
Named after Karl Reimer
Ferdinand Tiemann
Reaction type Substitution reaction
Identifiers
RSC ontology ID RXNO:0000072

The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols;[1][2][3][4][5] with the simplest example being the conversion of phenol to salicylaldehyde. The reaction was discovered by Karl Reimer (de)[6] and Ferdinand Tiemann. The Reimer in question was Karl Reimer (1845-1883) not the less known Carl Ludwig Reimer (1856-1921).[7]

The Reimer-Tiemann reaction

Reaction mechanism[edit]

The mechanism of the Reimer-Tiemann reaction

Chloroform (1) is deprotonated by a strong base (normally hydroxide) to form the chloroform carbanion (2) which will quickly alpha-eliminate to give dichlorocarbene (3); this is the principal reactive species. The hydroxide will also deprotonate the phenol (4) to give a negatively charged phenoxide (5). The negative charge is delocalised into the aromatic ring, making it far more nucleophilic. Nucleophilic attack of the dichlorocarbene gives an intermediate dichloromethyl substituted phenol (7). After basic hydrolysis, the desired product (9) is formed.[8]

Selectivity[edit]

By virtue of its 2 electron-withdrawing chlorine groups, carbine (3) is highly electron deficient and is attracted to the electron rich phenoxide (5). This interaction favors selective ortho-forymation.

Reaction conditions[edit]

Hydroxides are not readily soluble in the chloroform, thus the reaction is generally carried out in a biphasic solvent system. In the simplest sense this consists of an aqueous hydroxide solution and an organic phase containing the chloroform. The two reagents are therefore separated and must be brought together for the reaction to take place. This can be achieved by rapid mixing, phase-transfer catalysts, or an emulsifying agent (the use of 1,4-Dioxane as a solvent is an example).

The reaction typically needs to be heated to initiate the process, however once started the Reimer-Tiemann Reaction can be highly exothermic; this combination makes it prone to thermal runaways.

Scope[edit]

The Reimer–Tiemann reaction is effective for other hydroxy-aromatic compounds, such as naphthols.[9] Electron rich heterocycles such as pyrroles and indoles are also known to react.

Dichlorocarbenes can react with alkenes and amines to respectively form dichlorocyclopropanes and isocyanides. As such the Reimer-Tiemann reaction may be unsuitable for substrates bearing these functional groups. In addition, many compounds can not withstand being heated in the presence of hydroxide.

Comparison to other methods[edit]

The direct formylation of aromatic compounds can be accomplished by various methods such as the Gattermann reaction, Gattermann–Koch reaction, Vilsmeier–Haack reaction, or Duff reaction; however, in terms of ease and safety of operations, the Reimer–Tiemann reaction is often the most advantageous route chosen in chemical synthesis. Of the prior mentioned reactions, the Reimer–Tiemann reaction is the only route not requiring acidic and/or anhydrous conditions.[3] Additionally the Gattermann-Koch and Vilsmeier–Haack reactions are not applicable to phenol substrates.

Variations[edit]

The Reimer–Tiemann reaction can be altered to yield phenolic acids by substituting the chloroform with carbon tetrachloride.[10] For instance, the altered reaction with phenol would yield salicylic acid rather than the expected product, salicylaldehyde.

References[edit]

  1. ^ Reimer, K.; Tiemann, Ferd. (1876). "Ueber die Einwirkung von Chloroform auf Phenole und besonders aromatische Oxysäuren in alkalischer Lösung" [On the effect of chloroform on phenols and particularly aromatic oxyacids in alkaline solution]. Berichte der deutschen chemischen Gesellschaft. 9 (2): 1268–1278. doi:10.1002/cber.18760090270. 
  2. ^ Wynberg, Hans (1960). "The Reimer-Tiemann Reaction". Chemical Reviews. 60 (2): 169–184. doi:10.1021/cr60204a003. Retrieved 3 January 2014. 
  3. ^ a b Wynberg, Hans and Meijer, Egbert, Hans; Meijer, Egbert W. (2005). "The Reimer–Tiemann Reaction". Wiley Online Library: pg.14. doi:10.1002/0471264180.or028.01. ISBN 9780471264187. Retrieved 3 January 2014. 
  4. ^ Dauben, William G. (1982). Organic Reactions, Volume 28. Hoboken, NJ: Wiley-Interscience. p. 347. ISBN 978-0471861416. 
  5. ^ Wynberg, Hans (1991). "The Reimer–Tiemann Reaction". Comprehensive Organic Synthesis. 2 (Part 2): 769–775. doi:10.1016/B978-0-08-052349-1.00048-2. ISBN 978-0-08-052349-1. Retrieved 3 January 2014. 
  6. ^ Reimer, K. (1876). "Ueber eine neue Bildungsweise aromatischer Aldehyde" [On a new way of forming aromatic aldehydes]. Berichte der deutschen chemischen Gesellschaft (in German). 9: 423–424. 
  7. ^ see "Karl Reimer Nachruf 1883.pdf" at Commons and text on page 101.
  8. ^ Hine, Jack; Van Der Veen, James M. (December 1959). "The Mechanism of the Reimer-Tiemann Reaction". Journal of the American Chemical Society. 81 (24): 6446–6449. doi:10.1021/ja01533a028. 
  9. ^ Russell, Alfred; Lockhart, Luther B. (1942). "2-HYDROXY-1-NAPHTHALDEHYDE". Organic Syntheses. 22: 63. doi:10.15227/orgsyn.022.0063. 
  10. ^ Gaonkar, A.V.; Kirtany, J.K. (2010). "ChemInform Abstract: Reimer-Tiemann Reaction Using Carbon Tetrachloride". ChemInform. 22 (41): 1991. doi:10.1002/chin.199141092.