The Leuckart reaction is the chemical reaction that converts aldehydes or ketones to amines. The reaction is an example of reductive amination.[1] The reaction, named after Rudolf Leuckart, uses either ammonium formate or formamide as the nitrogen donor and reducing agent. It requires high temperatures, usually between 120 and 130 °C; for the formamide variant, the temperature can be greater than 165 °C.
| Leuckart reaction | |
|---|---|
| Named after | Rudolf Leuckart |
| Reaction type | Substitution reaction |
| Identifiers | |
| RSC ontology ID | RXNO:0000101 |
History
editThe Leuckart reaction is named in honor of its developer, the German chemist Rudolf Leuckart (1854–1899). He discovered that heating benzaldehyde with formamide does not produce benzylidenediformamide as anticipated, but benzylamine.[2] In 1891, a colleague of Leuckart at the University of Göttingen, Otto Wallach, performed further reactions using alicyclic and terpenoid ketones as well as aldehydes, demonstrating the general application.[2] Over the course of the past century, chemists have discovered several methods to improve the yield of the reaction and carry it out under less strenuous conditions. Pollard and Young summarized various ways in which amines can be formed: using either formamide or ammonium formate, or both, or adding formic acid to formamide.[3] However, using just ammonium formate as the reagent produces the best yields.[4][3] Using formamide produces low yields compared to ammonium formate but yields can be increased by using large amount of formamide, or using ammonium formate, ammonium sulfate, and magnesium chloride as catalysts.[5]
Mechanism
editAmmonium formate as reagent
editAmmonium formate is a source formic acid and ammonia. Starting with nucleophilic attack on the carbonyl by the ammonia, the carbonyl is converted to the iminium ion:[6]
- NH4HCO2 ⇌ NH3 + HCO2H
- NH3 + R2C=O + HCO2H → R2C=NH+2 + HCO−2
The iminium is then reduced by the formate:
- R2C=NH+2 + HCO−2 → R2CH−NH2 + CO2
Formamide as reagent
edit
Formamide first nucleophilically attacks the carbonyl carbon. The oxygen is protonated by abstracting hydrogen from the nitrogen atom, subsequently forming a water molecule that leaves, forming N-formyl derivative, which is resonance stabilized.[3] Water hydrolyzes formamide to give ammonium formate, which acts as a reducing agent and adds on to the N-formyl derivative. Hydride shift occurs, resulting in loss of carbon dioxide. An ammonium ion is added forming an imine and releasing ammonia. The imine goes through hydrolysis to form the amine, which is depicted in the scheme below.
Applications
editAn example of the Leuckart reaction is its use in the synthesis of tetrahydro-1,4 benzodiazepin-5-one, a molecule that is part of the benzodiazepine family.[7]
See also
editFurther reading
edit- Leuchart's finding that benzaldehyde and acetamide react to give tribenzylamine:Leuckart, R. (1885). "Ueber eine neue Bildungsweise von Tribenzylamin". Berichte der Deutschen Chemischen Gesellschaft. 18 (2): 2341–2344. doi:10.1002/cber.188501802113.
- Leuchart's use of ammonium formate:Leuckart, R.; Bach, E. (1886). "Ueber die Einwirkung von Ammoniumformiat auf Benzaldehyd und Benzophenon". Berichte der Deutschen Chemischen Gesellschaft. 19 (2): 2128–2131. doi:10.1002/cber.188601902105.</ref>
References
edit- ^ Moore, Maurice L. (2011). "The Leuckart Reaction". Organic Reactions. pp. 301–330. doi:10.1002/0471264180.or005.07. ISBN 978-0-471-26418-7.
- ^ a b Crossley, Frank S.; Maurice L. Moore (1944). "Studies on the Leuckart Reaction". Journal of Organic Chemistry. 9 (6): 529–536. doi:10.1021/jo01188a006.
- ^ a b c Pollard, C.B.; David C. Young (1951). "The Mechanism of the Leuckart Reaction". Journal of Organic Chemistry. 16 (5): 661–672. doi:10.1021/jo01145a001.
- ^ Alexander, Elliot; Ruth Bowman Wildman (1948). "Studies on the Mechanism of the Leuckart Reaction". Journal of the American Chemical Society. 70 (3): 1187–1189. doi:10.1021/ja01183a091. PMID 18909189.
- ^ Webers, Vincent J.; William F. Bruce (1948). "The Leuckart Reaction: A study of the Mechanism". Journal of the American Chemical Society. 70 (4): 1422–1424. doi:10.1021/ja01184a038. PMID 18915755.
- ^ Ingersoll, A. W. (1937). "α-Phenylethylamine". Organic Syntheses. 17: 76. doi:10.15227/orgsyn.017.0076.
- ^ Lee, Sung-Chan; Seung Bum Park (2007). "Novel application of Leuckart–Wallach reaction for synthesis of tetrahydro-1,4-benzodiazepin-5-ones library". Chemical Communications (36): 3714–3716. doi:10.1039/B709768A. PMID 17851604.