A Hydrazone Ligand for Iridium-Catalyzed C–H Borylation: Enhanced Reactivity and Selectivity for Fluorinated Arenes

• Published in: Organometallics Vol. 43; no. 11; pp. 1208 - 1212
• Main Authors: Peruzzi, Christopher D., Miller, Susanne L., Dannatt, Jonathan E., Ghaffari, Behnaz, Maleczka, Robert E., Smith, Milton R.
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 10.06.2024; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Inorganic & Nuclear; Chemistry, Organic; Communication; Physical Sciences; Science & Technology; FUNCTIONALIZATION; REGIOSELECTIVE BORYLATION; METAL; SPHERE; DIBORON
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/acs.organomet.4c00174

Ir-catalyzed C–H borylations of fluorinated and cyanated arenes with high meta-to-F/CN are described. Use of a dipyridyl hydrazone framework as the ancillary ligand and pinacolborane (HBpin) as the functionalizing reagent generates catalysts that are significantly more active and selective than 4,4′-di-tert-butyl-2,2′-bipyridine (dtbpy) for both electron-deficient and electron-rich substrates. Investigation of the ligand framework resulted in the observation of formal N-borylation of the hydrazone by HBpin, as evidenced by NMR spectroscopy and X-ray crystallography. Subsequent stoichiometric reactions of this adduct with an iridium precatalyst revealed the formation of an unusual IrI hydrazido. Isolation and use of this hydrazido reproduce the selectivity of in situ generated catalysts, suggesting that it leads to formation of the active species.