Decoding the Mechanism of Intramolecular Cu-Directed Hydroxylation of sp3 C–H Bonds

• Published in: Journal of organic chemistry 2017-08, Vol.82 (15), p.7887-7904
• Main Authors: Trammell, Rachel, See, Yi Yang, Herrmann, Aaron T, Xie, Nan, Díaz, Daniel E, Siegler, Maxime. A, Baran, Phil S, Garcia-Bosch, Isaac
• Format: Article
• Language: English
• ISSN: 0022-3263; 1520-6904; 1520-6904
• DOI: 10.1021/acs.joc.7b01069

The use of copper in directed C–H oxidation has been relatively underexplored. In a seminal example, Schönecker showed that copper and O2 promoted the hydroxylation of steroid-containing ligands. Recently, Baran (J. Am. Chem. Soc. 2015, 137, 13776) improved the reaction conditions to oxidize similar substrates with excellent yields. In both reports, the involvement of Cu2O2 intermediates was suggested. In this collaborative article, we studied the hydroxylation mechanism in great detail, resulting in the overhaul of the previously accepted mechanism and the development of improved reaction conditions. Extensive experimental evidence (spectroscopic characterization, kinetic analysis, intermolecular reactivity, and radical trap experiments) is provided to support each of the elementary steps proposed and the hypothesis that a key mononuclear LCuII(OOR) intermediate undergoes homolytic O–O cleavage to generate reactive RO• species, which are responsible for key C–H hydroxylation within the solvent cage. These key findings allowed the oxidation protocol to be reformulated, leading to improvements of the reaction cost, practicability, and isolated yield.