Chemistry:Stahl oxidation

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The Stahl oxidation is a copper-catalyzed aerobic oxidation of primary and secondary alcohols to aldehydes and ketones. Known for its high selectivity and mild reaction conditions, the Stahl oxidation offers several advantages over classical alcohol oxidations.

Key features of the Stahl oxidation are the use of a 2,2'-bipyridyl-ligated copper(I) species in the presence of a nitroxyl radical and N-methyl imidazole in polar aprotic solvent, most commonly acetonitrile or acetone.[1][2][3] Copper(I) sources can vary, though sources with non-coordinating anions like triflate, tetrafluoroborate, and hexafluorophosphate are preferred,[1] with copper(I) bromide[2] and copper(I) iodide[4] salts demonstrating utility in select applications. Frequently, tetrakis(acetonitrile)copper(I) salts are used.[1][5][6][7] For most applications, reactions can be run at room temperature and ambient air contains sufficiently high enough oxygen concentrations to be used as the terminal oxidant. Compared to chromium-, DMSO-, or periodinane-mediated oxidations, this proves safe, environmentally-friendly, practical, and highly economical.[8]

Model substrate used in Hoover & Stahl's seminal work. Under these conditions, >98% yields were observed by gas chromatography.[9]

In general, the Stahl oxidation is selective for oxidizing primary alcohols over secondary alcohols (both aliphatic and benzylic), and favors the oxidation of primary benzylic alcohols over primary aliphatic alcohols when TEMPO is used as the nitroxyl radical.[1] This is in contrast to the Oppenauer oxidation, which favors the oxidation of secondary alcohols over primary and several other specialty oxidations.[10][11] Over-oxidation of primary alcohols to carboxylic acids is rare, though lactones can form in certain diol-containing substrates.[1][3][7] The use of less hindered nitroxyl radicals like ABNO[12] or AZADO[13] allow for the oxidation of both primary and secondary alcohols.[14][15]

History

In 2011, Jessica Hoover and Shannon Stahl disclosed improved conditions for selective oxidation of primary alcohols to aldehydes using a (bpy)copper(I)/TEMPO system.[1] While several catalytic aerobic oxidation systems were known at the time, many utilized palladium, which can be prohibitive through its expense[16] and its cross-reactivity with alkene-bearing substrates.[17][18] Aerobic oxidative catalysis of alcohols by copper, though known since at least 1984,[19] was generally lower performing, requiring some combination of elevated reaction temperatures, higher catalyst loading, handling of pure oxygen, and biphasic or otherwise non-common solvent systems.[20][21][22]

Following the success of this initial disclosure, Hoover and Stahl went on to publish a further simplified protocol for rapid benzylic alcohol oxidation with Nicolas Hill, director of undergraduate organic chemistry laboratories at the University of Wisconsin - Madison.[2][23] Utilizing a less expensive solvent and copper source, Hill, Hoover, and Stahl demonstrated that higher catalyst loadings could be economically achieved. In doing so, the oxidation of alcohols could be accelerated for use as a practical educational tool in undergraduate labs. Furthermore, reaction completion is typically indicated by a change in solution color for red/brown to green resulting from a change in the copper species' resting state.[2] This is unique for benzylic and other activated alcohols, as the rate-limiting-step for these substrates is catalyst re-oxidation, which differs from aliphatic alcohols where the rate limiting step is C-H cleavage.[24] The Stahl oxidation is a component of the undergraduate organic chemistry laboratory curriculum at UW-Madison and the University of Utah.[25]

In 2013, the mechanism for the copper(I)/TEMPO oxidation of alcohols was elucidated,[24] and it was found the use of less hindered nitroxyl radical sources allowed for the oxidation of secondary alcohols.[14]

Modifications

Hoover–Stahl Oxidation of a primary benzylic alcohol on gram scale. Conditions - 3 mol% CuBr, 2,2'-bipyridyl, TEMPO; 6 mol% NMI; 0.2M in acetone. Left image: Time = 0 hr; Right image: Time = 12 hr. Note the change in brown to green color indicating a change in the resting state for the copper species.

Hoover–Stahl oxidation

The Hoover–Stahl oxidation explicitly indicates the earliest of the Stahl oxidation conditions allowing for the selective oxidation of primary alcohols. The system utilizes 2,2'-bipyridine (bpy), a copper(I) source (typically tetrakis(acetonitrile) copper(I) triflate, tetrafluoroborate, or hexafluorophosphate), TEMPO, and N-methylimidazole. The reaction is conducted in acetonitrile at room temperature under an atmosphere or air. Catalyst loadings are typically around 5 mol %, with N-methylimidazole being used at 10 mol %. The reaction is selective for oxidation of primary alcohols to aldehydes and generally does not oxidize secondary alcohols.[1] Solutions for the Hoover–Stahl oxidation are commercially available from Millipore-Sigma, though the catalyst can be easily prepared in situ from common laboratory reagents.[1][26]

Steves–Stahl oxidation

The Steves–Stahl oxidation indicates the use of a less hindered nitroxyl radical in the Stahl oxidation, allowing for the oxidation of secondary alcohols in addition to primary alcohols.[14] The reaction is conducted in acetonitrile at room temperature under an atmosphere of air, or less commonly, under an atmosphere of oxygen. Typically, the nitroxyl radical used in the Steves–Stahl is 9-Azabicyclo[3.3.1]nonane N-Oxyl (ABNO)[12] and is used in conjunction with a more strongly electron-donating 2,2'-bipyridyl ligand compared to bpy, like 4,4'-dimethoxy-2,2'-bipyridine, as this is shown to accelerate alcohol oxidation.[14] Due to the comparatively high price and reactivity of ABNO, common practice is to use it sparingly, oftentimes at catalytic loading of 1 mol % or less.[27] Solutions for the Steves–Stahl oxidation are commercially available through Millipore-Sigma, though the mixture can be easily prepared in situ.[28] Due to the high reagent cost associated with the Steves–Stahl oxidation, it is generally only employed for oxidation of secondary alcohols or after the Hoover–Stahl oxidation has proved fruitless. Several improved methods for the scalable preparation of ABNO have been recently published.[29][30]

Xie–Stahl oxidative lactonization

The Xie–Stahl oxidative lactonization is a lactonization reaction which generally employs Steves–Stahl conditions for the oxidative cyclization of diols.[3] The Xie–Stahl reaction lends itself toward selective formation of γ-, δ-, and ε-lactones, forming the carbonyl at the less-hindered primary alcohol. In some instances, higher selectivity can be afforded through the use of 1 mol % TEMPO in place of ABNO.[3]

Zultanski–Zhao–Stahl oxidative amide coupling

The Zultanski–Zhao–Stahl oxidative amide coupling is a reaction between a primary alcohol and an amine to form an amide.[31] In the Zultanski–Zhao–Stahl reaction, a primary alcohol is oxidized to an aldehyde which, in the presence of an amine, reversibly forms a hemiaminal which is then irreversibly oxidized to the amide by the catalyst. The reaction is performed under an atmosphere of oxygen in the presence of 3Å molecular sieves using relatively high ABNO loading of 3 mol %. Optimal reaction conditions are substrate dependent, requiring specific copper(I) sources, ligands, and solvents depending on the structure of the starting alcohol and amines.[31]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Hoover, Jessica M.; Stahl, Shannon S. (2011-10-26). "Highly Practical Copper(I)/TEMPO Catalyst System for Chemoselective Aerobic Oxidation of Primary Alcohols" (in en). Journal of the American Chemical Society 133 (42): 16901–16910. doi:10.1021/ja206230h. ISSN 0002-7863. PMID 21861488. 
  2. ↑ 2.0 2.1 2.2 2.3 Hill, Nicholas J.; Hoover, Jessica M.; Stahl, Shannon S. (2013-01-08). "Aerobic Alcohol Oxidation Using a Copper(I)/TEMPO Catalyst System: A Green, Catalytic Oxidation Reaction for the Undergraduate Organic Chemistry Laboratory" (in en). Journal of Chemical Education 90 (1): 102–105. doi:10.1021/ed300368q. ISSN 0021-9584. Bibcode: 2013JChEd..90..102H. 
  3. ↑ 3.0 3.1 3.2 3.3 Xie, Xiaomin; Stahl, Shannon S. (2015-03-25). "Efficient and Selective Cu/Nitroxyl-Catalyzed Methods for Aerobic Oxidative Lactonization of Diols" (in en). Journal of the American Chemical Society 137 (11): 3767–3770. doi:10.1021/jacs.5b01036. ISSN 0002-7863. PMID 25751494. 
  4. ↑ Ochen, Augustine; Whitten, Robert; Aylott, Helen E.; Ruffell, Katie; Williams, Glynn D.; Slater, Fiona; Roberts, Andrew; Evans, Paul et al. (2019-01-14). "Development of a Large-Scale Copper(I)/TEMPO-Catalyzed Aerobic Alcohol Oxidation for the Synthesis of LSD1 Inhibitor GSK2879552" (in en). Organometallics 38 (1): 176–184. doi:10.1021/acs.organomet.8b00546. ISSN 0276-7333. 
  5. ↑ Forster, Michael; Chaikuad, Apirat; Dimitrov, Teodor; Döring, Eva; Holstein, Julia; Berger, Benedict-Tilman; Gehringer, Matthias; Ghoreschi, Kamran et al. (2018-05-31). "Development, Optimization, and Structure–Activity Relationships of Covalent-Reversible JAK3 Inhibitors Based on a Tricyclic Imidazo[5,4-d]pyrrolo[2,3-b]pyridine Scaffold". Journal of Medicinal Chemistry 61 (12): 5350–5366. doi:10.1021/acs.jmedchem.8b00571. ISSN 0022-2623. PMID 29852068. 
  6. ↑ Lowell, Andrew N.; DeMars, Matthew D.; Slocum, Samuel T.; Yu, Fengan; Anand, Krithika; Chemler, Joseph A.; Korakavi, Nisha; Priessnitz, Jennifer K. et al. (2017-06-14). "Chemoenzymatic Total Synthesis and Structural Diversification of Tylactone-Based Macrolide Antibiotics through Late-Stage Polyketide Assembly, Tailoring, and C—H Functionalization" (in en). Journal of the American Chemical Society 139 (23): 7913–7920. doi:10.1021/jacs.7b02875. ISSN 0002-7863. PMID 28525276. 
  7. ↑ 7.0 7.1 Alfonzo, Edwin; Beeler, Aaron B. (2019). "A sterically encumbered photoredox catalyst enables the unified synthesis of the classical lignan family of natural products" (in en). Chemical Science 10 (33): 7746–7754. doi:10.1039/C9SC02682G. ISSN 2041-6520. PMID 31588322. 
  8. ↑ US EPA, OCSPP (2014-09-30). "Presidential Green Chemistry Challenge: 2014 Academic Award" (in en). https://www.epa.gov/greenchemistry/presidential-green-chemistry-challenge-2014-academic-award. 
  9. ↑ Hoover, Jessica M.; Stahl, Shannon S. (2011-10-26). "Highly Practical Copper(I)/TEMPO Catalyst System for Chemoselective Aerobic Oxidation of Primary Alcohols" (in en). Journal of the American Chemical Society 133 (42): 16901–16910. doi:10.1021/ja206230h. ISSN 0002-7863. PMID 21861488. 
  10. ↑ Mello, Rossella; Martínez-Ferrer, Jaime; Asensio, Gregorio; González-Núñez, María Elena (November 2007). "Oppenauer Oxidation of Secondary Alcohols with 1,1,1-Trifluoroacetone as Hydride Acceptor" (in en). The Journal of Organic Chemistry 72 (24): 9376–9378. doi:10.1021/jo7016422. ISSN 0022-3263. PMID 17975928. 
  11. ↑ Tojo, Gabriel. (2006). Oxidation of alcohols to aldehydes and ketones : a guide to current common practice. Fernández, Marcos (Marcos I.). New York, NY: Springer. ISBN 978-0-387-23607-0. OCLC 190867041. https://www.worldcat.org/oclc/190867041. 
  12. ↑ 12.0 12.1 "9-Azabicyclo[3.3.1nonane N-Oxyl, ABNO"]. https://www.organic-chemistry.org/chemicals/oxidations/9-azabicyclo%5B3.3.1%5Dnonane-N-oxyl-abno.shtm. 
  13. ↑ "2-Azaadamantane N-Oxyl, AZADO". https://www.organic-chemistry.org/chemicals/oxidations/2-azaadamantane-n-oxyl-azado.shtm. 
  14. ↑ 14.0 14.1 14.2 14.3 Steves, Janelle E.; Stahl, Shannon S. (2013-10-23). "Copper(I)/ABNO-Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems" (in en). Journal of the American Chemical Society 135 (42): 15742–15745. doi:10.1021/ja409241h. ISSN 0002-7863. PMID 24128057. 
  15. ↑ Ryland, Bradford L.; Stahl, Shannon S. (2014-08-18). "Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems" (in en). Angewandte Chemie International Edition 53 (34): 8824–8838. doi:10.1002/anie.201403110. PMID 25044821. 
  16. ↑ "Live USD Palladium Price Charts & Historical Data" (in en). https://www.apmex.com/palladium-price. 
  17. ↑ Nishimura, Takahiro; Kakiuchi, Nobuyuki; Onoue, Tomoaki; Ohe, Kouichi; Uemura, Sakae (2000). "Palladium(II)-catalyzed oxidation of terminal alkenes to methyl ketones using molecular oxygen". Journal of the Chemical Society, Perkin Transactions 1 (12): 1915–1918. doi:10.1039/b001854f. http://xlink.rsc.org/?DOI=b001854f. 
  18. ↑ Mifsud, Maria; Parkhomenko, Ksenia V.; Arends, Isabel W.C.E.; Sheldon, Roger A. (January 2010). "Pd nanoparticles as catalysts for green and sustainable oxidation of functionalized alcohols in aqueous media" (in en). Tetrahedron 66 (5): 1040–1044. doi:10.1016/j.tet.2009.11.007. 
  19. ↑ Semmelhack, M. F.; Schmid, Christopher R.; Cortes, David A.; Chou, Chuen S. (May 1984). "Oxidation of alcohols to aldehydes with oxygen and cupric ion, mediated by nitrosonium ion" (in en). Journal of the American Chemical Society 106 (11): 3374–3376. doi:10.1021/ja00323a064. ISSN 0002-7863. 
  20. ↑ Gamez, Patrick; Arends, Isabel W. C. E.; Reedijk, Jan; Sheldon, Roger A. (2003). "Copper(ii)-catalysed aerobic oxidation of primary alcohols to aldehydes" (in en). Chemical Communications (19): 2414–5. doi:10.1039/b308668b. ISSN 1359-7345. PMID 14587708. http://xlink.rsc.org/?DOI=b308668b. 
  21. ↑ Ragagnin, Gianna; Betzemeier, Bodo; Quici, Silvio; Knochel, Paul (May 2002). "Copper-catalysed aerobic oxidation of alcohols using fluorous biphasic catalysis" (in en). Tetrahedron 58 (20): 3985–3991. doi:10.1016/S0040-4020(02)00250-8. 
  22. ↑ Marko, I. E.; Giles, P. R.; Tsukazaki, M.; Brown, S. M.; Urch, C. J. (1996-12-20). "Copper-Catalyzed Oxidation of Alcohols to Aldehydes and Ketones: An Efficient, Aerobic Alternative". Science 274 (5295): 2044–2046. doi:10.1126/science.274.5295.2044. ISSN 0036-8075. PMID 8953027. Bibcode: 1996Sci...274.2044M. 
  23. ↑ "hill | UW-Madison Department of Chemistry" (in en-us). https://www.chem.wisc.edu/users/hill. 
  24. ↑ 24.0 24.1 Hoover, Jessica M.; Ryland, Bradford L.; Stahl, Shannon S. (2013-02-13). "Mechanism of Copper(I)/TEMPO-Catalyzed Aerobic Alcohol Oxidation" (in en). Journal of the American Chemical Society 135 (6): 2357–2367. doi:10.1021/ja3117203. ISSN 0002-7863. PMID 23317450. 
  25. ↑ "Experiment 15: Aerobic Oxidation of an Alcohol Using a Cu/TEMPO Catalyst System | UW-Madison Department of Chemistry". https://www.chem.wisc.edu/content/experiment-15-aerobic-oxidation-alcohol-using-cutempo-catalyst-system. 
  26. ↑ "Stahl Aerobic Oxidation TEMPO solution 796549". https://www.sigmaaldrich.com/catalog/product/aldrich/796549. 
  27. ↑ Steves, Janelle E.; Preger, Yuliya; Martinelli, Joseph R.; Welch, Christopher J.; Root, Thatcher W.; Hawkins, Joel M.; Stahl, Shannon S. (2015-07-15). "Process Development of CuI/ABNO/NMI-Catalyzed Aerobic Alcohol Oxidation". Organic Process Research & Development 19 (11): 1548–1553. doi:10.1021/acs.oprd.5b00179. ISSN 1083-6160. 
  28. ↑ "Stahl Aerobic Oxidation ABNO solution 796557". https://www.sigmaaldrich.com/catalog/product/aldrich/796557. 
  29. ↑ Shibuya, Masatoshi; Tomizawa, Masaki; Sasano, Yusuke; Iwabuchi, Yoshiharu (2009-06-19). "An Expeditious Entry to 9-Azabicyclo[3.3.1]nonane N -Oxyl (ABNO): Another Highly Active Organocatalyst for Oxidation of Alcohols" (in en). The Journal of Organic Chemistry 74 (12): 4619–4622. doi:10.1021/jo900486w. ISSN 0022-3263. PMID 19476345. 
  30. ↑ Song, Zhiguo J.; Zhou, Guoyue; Cohen, Ryan; Tan, Lushi (2018-09-21). "Preparation of ABNO on Scale and Analysis by Quantitative Paramagnetic NMR" (in en). Organic Process Research & Development 22 (9): 1257–1261. doi:10.1021/acs.oprd.8b00191. ISSN 1083-6160. 
  31. ↑ 31.0 31.1 Zultanski, Susan L.; Zhao, Jingyi; Stahl, Shannon S. (2016-05-25). "Practical Synthesis of Amides via Copper/ABNO-Catalyzed Aerobic Oxidative Coupling of Alcohols and Amines" (in en). Journal of the American Chemical Society 138 (20): 6416–6419. doi:10.1021/jacs.6b03931. ISSN 0002-7863. PMID 27171973. 

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