The reaction is closely related to the Curtius rearrangement except that in this reaction the acyl azide is produced by reaction of the carboxylic acid with hydrazoic acid via the protonated carboxylic acid, in a process akin to a Fischer esterification. An alternative, involving the formation of an acylium ion, becomes more important when the reaction takes place in concentrated acid (>90% sulfuric acid).[7] (In the Curtius rearrangement, sodium azide and an acyl chloride are combined to quantitatively generate the acyl azide intermediate, and the rest of the reaction takes place under neutral conditions.)
The carboxylic acid Schmidt reaction starts with acylium ion 1 obtained from protonation and loss of water. Reaction with hydrazoic acid forms the protonated azido ketone 2, which goes through a rearrangement reaction with the alkyl group R, migrating over the C-N bond with expulsion of nitrogen. The protonated isocyanate is attacked by water forming carbamate4, which after deprotonation loses carbon dioxide to the amine.
In the reaction mechanism for the Schmidt reaction of ketones, the carbonyl group is activated by protonation for nucleophilic addition by the azide, forming azidohydrin 3, which loses water in an elimination reaction to diazoiminium 5. One of the alkyl or aryl groups migrates from carbon to nitrogen with loss of nitrogen to give a nitrilium intermediate 6, as in the Beckmann rearrangement. Attack by water converts 6 to protonated imidic acid 7, which undergoes loss of proton to arrive at the imidic acid tautomer of the final amide. In an alternative mechanism, the migration occurs at 9, directly after protonation of intermediate 3, in a manner similar to the Baeyer–Villiger oxidation to give protonated amide 10. Loss of a proton again furnishes the amide. It has been proposed that the dehydration to 3 to give 5 (and, hence, the Beckmann pathway) is favored by nonaqueous acids like conc. H2SO4, while aqueous acids like conc. HCl favor migration from 9 (the Baeyer-Villiger pathway). These possibilities have been used to account for the fact that, for certain substrates like α-tetralone, the group that migrates can sometimes change, depending on the conditions used, to deliver either of the two possible amides.[8]
Reactions involving alkyl azides
The scope of this reaction has been extended to reactions of carbonyls with alkyl azides R-N3. This extension was first reported by J.H. Boyer in 1955 [9] (hence the name Boyer reaction), for example, the reaction of 3-nitrobenzaldehyde with β-azido ethanol:
Variations involving intramolecular Schmidt reactions have been known since 1991.[5] These are annulation reactions and have some utility in the synthesis of natural products;[6][10] such as lactams[11] and alkaloids.[12]
^Lang, S.; Murphy, J. A. (2006). "Azide rearrangements in electron-deficient systems". Chem. Soc. Rev. 35 (2): 146–156. doi:10.1039/B505080D. PMID16444296.
^Schmidt, K. F. (1924). "Über den Imin-Rest". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 57 (4): 704–723. doi:10.1002/cber.19240570423.
^Crosby, Ian T.; Shin, James K.; Capuano, Ben (2010). "The Application of the Schmidt Reaction and Beckmann Rearrangement to the Synthesis of Bicyclic Lactams: Some Mechanistic Considerations". Australian Journal of Chemistry. 63 (2): 211. doi:10.1071/CH09402. ISSN0004-9425.
^J. H. Boyer & J. Hamer (1955). "The Acid-catalyzed Reaction of Alkyl Azides upon Carbonyl Compounds". J. Am. Chem. Soc.77 (4): 951–954. doi:10.1021/ja01609a045.
^Milligan, Gregory L.; Mossman, Craig J.; Aube, Jeffrey (October 1995). "Intramolecular Schmidt Reactions of Alkyl Azides with Ketones: Scope and Stereochemical Studies". Journal of the American Chemical Society. 117 (42): 10449–10459. doi:10.1021/ja00147a006.
^Wrobleski, Aaron; Sahasrabudhe, Kiran; Aubé, Jeffrey (May 2004). "Asymmetric Total Synthesis of Dendrobatid Alkaloids: Preparation of Indolizidine 251F and Its 3-Desmethyl Analogue Using an Intramolecular Schmidt Reaction Strategy". Journal of the American Chemical Society. 126 (17): 5475–5481. doi:10.1021/ja0320018. PMID15113219.