Copper hydride-mediated electrophilic amidation of vinylarenes with dioxazolones - a computational mechanistic study

• Published in: Dalton transactions : an international journal of inorganic chemistry 2019-10, Vol.48 (38), p.14337-14346
• Main Author: Tobisch, Sven
• Format: Article
• Language: English
• Subjects: Benzene; Catalysis; Catalysts; Copper; Copper converters; Decarboxylation; Hydrides; Styrenes
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c9dt02540e

A detailed computational mechanistic study of the CuH-catalysed formal hydroamidation of vinylarenes with dioxazolone and hydrosilane by a prototype (dppbz)CuH catalyst (dppbz ≡ {P^P} ≡ 1,2-bis(diphenylphosphino)benzene) is presented. Probing various plausible pathways for relevant elementary steps with the aid of a reliable computational protocol applied to a realistic catalyst model identified the pathways preferably traversed in productive catalysis. It entails hydrocupration exclusively generating the benzylcopper nucleophile that undergoes amidation with the dioxazolone electrophile to afford copper amidate. Umpolung electrophilic amidation favours a stepwise oxidative Cu&z.dbd;N coupling with a simultaneous decarboxylation/C-N bond forming reductive elimination sequence. Copper amidate represents the catalyst resting state. Its conversion back into the catalytically active copper hydride upon transmetalation with hydrosilane involves fast nucleophilic attack followed by slow hydrogen atom transfer. Electron-poor styrenes accelerate the hydrocupration with a noticeably reduced barrier found for styrene featuring a para -CF 3 substituted phenyl ring. On the other hand, transmetalation becomes faster the more electron-rich the oxazolone amidating agent is. An in-depth computational mechanistic probe of the CuH-mediated formal hydroamidation of vinylarenes with dioxazolones allowed the substitution of mechanistic hypothesis advanced previously by a computationally verified mechanistic view.