Wallach rearrangement
The Wallach rearrangement, also named Wallach transformation, is a name reaction in the organic chemistry. It is named after Otto Wallach, who discovered this reaction in 1880. In general it is a strong acid-promoted conversion of azoxybenzenes into hydroxyazobenzenes.[1][2][3]
General Reaction Scheme
The Wallach rearrangement is an organic reaction converting an aromatic azoxy compound with sulfuric acid or other strong acids to an azo compound with one arene ring substituted by a hydroxyl group in the aromatic para position.[4]
Conceptually related reactions are the Fries rearrangement, the Fischer–Hepp rearrangement, the Bamberger rearrangement, the benzidine rearrangement and the Hofmann–Martius rearrangement.
In the first part of the reaction, two equivalents of acid tease the oxygen atom away from the azoxy group. The resulting dicationic intermediate with an unusual R–N+=N+–R motif in this scheme has been observed by proton NMR in a system of fluoroantimonic acid and azoxybenzene at −50 °C.[5] In the second part, the HSO4− anion is a nucleophile in a nucleophilic aromatic substitution followed by hydrolysis.
Reaction Mechanism
The reaction mechanism for this reaction is not known with great precision despite experimental evidence:
- The primary kinetic isotope effect for the arene proton is close to one excluding the corresponding C–H bond from breaking in the rate-determining step.
- The chemical kinetics of the reaction point to involvement of two protons in the reaction: the reaction rate of the rearrangement continues to increase beyond the stage of complete monoprotonation of the substrate.
- Other kinetic evidence identifies the second proton donation as the rate-determining step.
- The phenolic oxygen atom in the product is not the oxygen atom in the reactant but provided by solvent, based on isotopic scrambling experiments.
- Furthermore, isotope labeling of the N–O nitrogen atom in azoxybenzene gives the azo compound with the 15N isotope distributed over both nitrogen atoms indicating a symmetrical intermediate.
A mechanism not inconsistent with these findings is depicted below:[2]
First two hydrogen-atoms are added to the azoxybenzene (1). The first one goes to the negative charged oxygen-atom. The second one goes to the nitrogen-atom without bounded oxygen. After a condensation, a dicationic compound with two mesomers 2 is built. In the next step water is added and an oxonium ion (3) is built. After proton donation, the compound is aromatic again and the hydroxyazobenzene (4) is generated.
Applications
This reaction has a general application in the preparation of hydroxyazobenzenes and hydroxyazonaphthalenes. They are used for coloration of soap, lacquer and resin.
References
- ↑ Otto Wallach and E. Belli, Chem. Ber., 13, 525 (1880) doi:10.1002/cber.188001301153
- 1 2 Zerong Wang (2009) (in German), Comprehensive Organic Name Reactions and Reagents, New Jersey: John Wiley & Sons, pp. 2942 – 2945, ISBN 978-0-471-70450-8
- ↑ M. Windholz (1976) (in German), The Merck Index, Rakway: Merck&Co., pp. ONR-92, ISBN 0-911910-26-3
- ↑ Catalysis in strongly acidic media and the Wallach rearrangement Erwin Buncel Acc. Chem. Res.; 1975; 8(4) pp 132 – 139; doi:10.1021/ar50088a004
- ↑ Stable carbocations. CXXIX. Mechanism of the benzidine and Wallach rearrangements based on direct observation of dicationic reaction intermediates and related model compounds George A. Olah, Kenneth Dunne, David P. Kelly, Y. K. Mo J. Am. Chem. Soc.; 1972; 94(21); 7438–47.doi: 10.1021/ja00776a029