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Sodium Butylated Hydroxytoluene: A Functional Group Tolerant, Eco-Friendly Base for Solvent-Free, Pd-Catalysed Amination.
Semeniuchenko, Volodymyr; Braje, Wilfried M; Organ, Michael G.
Afiliação
  • Semeniuchenko V; Centre for Catalysis Research and Innovation (CCRI), Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N6N5, Canada.
  • Braje WM; AbbVie Deutschland GmbH & Co. KG, Neuroscience Discovery Research, Knollstrasse, 67061, Ludwigshafen, Germany.
  • Organ MG; Centre for Catalysis Research and Innovation (CCRI), Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N6N5, Canada.
Chemistry ; 27(49): 12535-12539, 2021 Sep 01.
Article em En | MEDLINE | ID: mdl-34190367
NaBHT (sodium 2,6-di-tert-butyl-4-methylphenolate), a strong, but hindered and lipophilic base, has been effectively paired with similarly lipophilic, high-reactivity Pd-NHC (N-heterocyclic carbene) catalysts to produce an ideal combination for performing solvent-free (melt) cross-coupling amination. The mild nucleophilicity of NaBHT, coupled with the anti-oxidant properties of its conjugate acid byproduct, BHT means the process seems to have no functional group incompatibilities. Highly effective coupling of base-sensitive and redox-active functional groups was observed in all cases with only 0.1-0.2 mol percent catalyst. Comparisons using the standard base for this reaction, KOtBu, led to poor couplings or complete degradation in most applications - only NaBHT works.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sódio / Hidroxitolueno Butilado Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sódio / Hidroxitolueno Butilado Idioma: En Ano de publicação: 2021 Tipo de documento: Article