Ugi's amine

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Ugi's amine
Ugi's amine R S.png
(R)- and (S)-enantiomers of Ugi's amine
IUPAC name
Other names
Molar mass 257.16 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Ugi’s amine is a chemical compound named for the chemist who first reported its synthesis in 1970, Ivar Ugi.[1] It is a ferrocene derivative, since its first report, Ugi’s amine has found extensive use as the synthetic precursor to a large number of metal ligands that bear planar chirality.[2] These ligands have since found extensive use in a variety of catalytic reactions, the compound may exist in either the 1S or 1R isomer, both of which have synthetic utility and are commercially available. Most notably, it is the synthetic precursor to the Josiphos class of ligands.


In 1967, Schlӧg repurposed the term “planar chirality” for use in substituted ferrocene terminology, which is necessary for ferrocenes in which ferrocene's innate plane of symmetry is broken by introducing two substituents to one of its ring.[3] Nozaki, et al. demonstrated that a ferrocene derivative bearing a chiral amine substituent could participate in directed ortho lithiation of the same ring of the ferrocene, yielding products with planar chirality diastereoselectively.[4] Nozaki’s ferrocene derivative provided products that were only 86% optically pure. Ugi, et al. improved the stereoselectivity by using [1-(dimethylamino)ethyl]-ferrocene, providing products that had an optical purity >95%. The utility of Ugi’s amine in forming ligands for asymmetric catalysis was first reported in 1974 by Kumada, et al.[5]


The first synthesis of Ugi’s amine was reported in 1970 by Ugi, et al. It begins by converting (±)1-ferrocenylethanol to (±)1-ferrocenylchloroethane. This is then substituted in situ with dimethylamine, resulting in a racemic mixture of [1-(dimethylamino)ethyl]-Ferrocene, the racemic mixture is subsequently resolved via recrystallization of the tartrate salt, providing both enantiomers in their enantio-pure form.[1]

Ugi's first report of the synthesis of [1-(dimethylamino)ethyl]-ferrocene.

Since the original report, other syntheses of Ugi’s amine have been reported, these are generally directed towards the synthesis of only one of the enantiomers rather than a racemic mixture. An enzymatic resolution of (±)1-ferrocenylethanol can be performed by Pseudomonas Fluorescens lipase-mediated acylation with vinyl acetate, providing unreacted (1S)-1-ferrocenylethanol (92% ee) and (1R)-[1-(acetyloxy)ethyl]-ferrocene (96% ee). The later can be easy hydrolyzed to (1R)-1-ferrocenylethanol.[6] Either stereoisomer of can be converted to Ugi’s amine first by conversion to the acetate, then displacement with dimethylamine with complete stereoretention (see below for stereochemical outcome). Additionally, Knochel, et al. reported a stereoselective synthesis of Ugi’s amine using the same acetylation/displacement strategy, but accesses (1R)-1-ferrocenylethanol from a Corey-Bakshi-Shibata reduction of acetylferrocene.[7]

Enzymatic resolution and stereoselective reduction in route to enantiopure Ugi's Amine.

Reactions of Ugi's Amine[edit]

Ugi’s amine is capable of promoting directed ortho lithiation diastereoselctively (with respect to planar chirality). [(1S)-(dimethylamino)ethyl]-ferrocene treated with n-BuLi, then quenched with TMSCl produces a planar chirality of (Rp). Treatment of [(1R)-(dimethylamino)ethyl]-ferrocene under these conditions produces a planar chirality of (Sp).[1][8] This selectivity is dictated by the orientation of the methyl substituent on the starting material in the conformation necessary for the nitrogen to be chelated to the lithiate; in one case this methyl substituent suffers from steric interactions with the other Cp ring, and in the other it points away from all other atoms. The high diastereoselectivity is independent of the electrophile used to trap the metalate, providing evidence for the stereoinductive step being lithiation and allowing broad synthetic utility of Ugi’s amine. If the (S,Sp) or (R,Rp) diastereomers are desired, the first metalate can be trapped with TMSCl to block the more favored lithiation position. Subsequent lithiation occurs at the only available, less favored site. Trapping with the desired electrophile and TBAF deprotection of the TMS group will provide the (S,Sp) or (R,Rp) diastereomer.

Rationale for the stereochemical outcome of directed lithiation of Ugi's Amine.

Further functionalization can take place at the carbon alpha to the ferrocene by substituting the dimethylamine with various nucleophiles, this is usually accomplished by quaternization of the amine with methyl iodide or acetic acid, which upon heating eliminates, resulting in a stable α-ferrocenylethyl cation intermediate. Addition of nucleophiles results substitution that is usually completely stereoretentive. Amines, carboxylates, alcohols, thiols, and posphines are all competent nucleophiles,[1][9] this is a common phenomenon for α-substituted ferrocenes.[10]

Substitution of Ugi's Amine with stereoretention.

Ligands From Ugi's Amine[edit]

Ugi’s amine has found extensive use in the synthesis of metal binding ligands used in homogeneous catalysis, as its ring-substituted derivatives generally contain a chiral center as well as planar chirality, it often produces high levels of enantioinduction in these reactions. The these two forms of chirality, in some cases, is thought to work synergistically for enantioinduction,[11] it is most commonly substituted with phosphorus to provide mono-, bi-, and tridentate phosphine ligands. The first report of such ligands was Kumada’s 1974 report of four mono- and bisphosphine ligands used for the rhodium-catalyzed asymmetric hydrosilation of ketones,[5] the most notable set of ligands synthesized from Ugi’s amine is the Josiphos class of ligands, which has found use in numerous catalytic reaction types[12] on both small and large scales.[13] Below is a list of representative ligands derived from Ugi's amine:[2]

  • Josiphos[13]
  • Pigiphos
  • TRAP
  • Walphos
  • BoPhoz
  • Xyliphos
  • Taniaphos

Asymmetric Reactions Utilizing Ligands Derived From Ugi's Amine[edit]

Reaction Type Metal Center(s)
Hydrosilation of ketones[5] Ru
Grignard Addition[14] Ni
Reduction of activated alkenes[15][16] Ru, Cu
Reduction of enamides[13] Ru
Reduction of ketones[17] Ru, Ir
Transfer hydrogenation of ketones[18] Re
Hydroalkynylation of allenes[19] Co
Allylic substitution[20] Pd
Coupling of ketoamides to aldehydes[21] Rh
Conjugate addition[22] Cu
Baylis-Hillman reaction[23] N/A (H-bonding)
[3+2] cycloaddition[24] Cu
Hydroboration[25] Cu


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  8. ^ Battelle, Linda F.; Bau, Robert.; Gokel, George W.; Oyakawa, Ray T.; Ugi, Ivar K. (1973-01-01). "Stereoselective synthesis. VIII. Absolute configuration of a 1,2-disubstituted ferrocene derivative with planar and central elements of chirality and the mechanism of the optically active .alpha.-ferrocenyl tertiary amines". Journal of the American Chemical Society. 95 (2): 482–486. doi:10.1021/ja00783a030. ISSN 0002-7863. 
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  12. ^ Blaser, Hans-Ulrich; Lotz, Matthias (2001-01-01). Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons, Ltd. doi:10.1002/047084289x.rn00874. ISBN 9780470842898. 
  13. ^ a b c Blaser, Hans-Ulrich (2002-01-01). "The Chiral Switch of (S)-Metolachlor: A Personal Account of an Industrial Odyssey in Asymmetric Catalysis". Advanced Synthesis & Catalysis. 344 (1): 17–31. doi:10.1002/1615-4169(200201)344:13.0.CO;2-8. ISSN 1615-4169. 
  14. ^ Hayashi, Tamio; Tajika, Masatoyo; Tamao, Kohei; Kumada, Makoto (1976-06-01). "High stereoselectivity in asymmetric Grignard cross-coupling catalyzed by nickel complexes of chiral (aminoalkylferrocenyl)phosphines". Journal of the American Chemical Society. 98 (12): 3718–3719. doi:10.1021/ja00428a061. ISSN 0002-7863. 
  15. ^ Lipshutz, Bruce H.; Servesko, Jeff M. (2003-10-13). "CuH-Catalyzed Asymmetric Conjugate Reductions of Acyclic Enones". Angewandte Chemie International Edition. 42 (39): 4789–4792. doi:10.1002/anie.200352313. ISSN 1521-3773. 
  16. ^ Shultz, C. Scott; Dreher, Spencer D.; Ikemoto, Norihiro; Williams, J. Michael; Grabowski, Edward J. J.; Krska, Shane W.; Sun, Yongkui; Dormer, Peter G.; DiMichele, Lisa (2005-08-01). "Asymmetric Hydrogenation of N-Sulfonylated-α-dehydroamino Acids:  Toward the Synthesis of an Anthrax Lethal Factor Inhibitor". Organic Letters. 7 (16): 3405–3408. doi:10.1021/ol050869s. ISSN 1523-7060. 
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  18. ^ Mejía, Esteban; Aardoom, Raphael; Togni, Antonio (2012-11-01). "Asymmetric Transfer Hydrogenation of Ketones Catalyzed by Rhenium Complexes with Chiral Ferrocenylphosphane Ligands". European Journal of Inorganic Chemistry. 2012 (31): 5021–5032. doi:10.1002/ejic.201200693. ISSN 1099-0682. 
  19. ^ Sawano, Takahiro; Ou, Keiyu; Nishimura, Takahiro; Hayashi, Tamio (2013-09-20). "Cobalt-Catalyzed Asymmetric Addition of Silylacetylenes to 1,1-Disubstituted Allenes". The Journal of Organic Chemistry. 78 (18): 8986–8993. doi:10.1021/jo401604n. ISSN 0022-3263. 
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  23. ^ Li, Chuang; Ma, Peng-Fei; Lei, Yang; Chen, Hui; Guan, Shao-Yu; Jiang, Ru; Chen, Wei-Ping (2016-08-01). "Enantioselective Morita–Baylis–Hillman Reaction of Acrylates with Nitrobenzaldehydes Promoted by the Bifunctional Ferrocene-Based Phosphinothiourea Organocatalysts". Catalysis Letters. 146 (8): 1429–1434. doi:10.1007/s10562-016-1759-9. ISSN 1011-372X. 
  24. ^ Han, Fu-Zhong; Yu, Sai-Bo; Zhang, Cheng; Hu, Xiang-Ping (2016-05-26). "Chiral ferrocenyl P,S-ligands for highly efficient copper-catalyzed asymmetric [3+2] cycloaddition of azomethine ylides". Tetrahedron. Chiral Sulfur Ligands/Catalysts in Asymmetric Catalysis. 72 (21): 2616–2622. doi:10.1016/j.tet.2015.01.003. 
  25. ^ Lee, Hyesu; Lee, Byoung Yoon; Yun, Jaesook (2015-02-06). "Copper(I)–Taniaphos Catalyzed Enantiodivergent Hydroboration of Bicyclic Alkenes". Organic Letters. 17 (3): 764–766. doi:10.1021/ol503598w. ISSN 1523-7060.