4.7 Article

One-Pot Synthesis of Substituted Benzo[b]furans and Indoles from Dichlorophenols/Dichloroanilines Using a Palladium - Dihydroxyterphenylphosphine Catalyst

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 81, Issue 13, Pages 5450-5463

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b00824

Keywords

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Funding

  1. JSPS [24750036, 15H04634, 15K18833]
  2. Society of Synthetic Organic Chemistry, Japan
  3. Uehara Memorial Foundation
  4. Platform Project for Supporting in Drug Discovery and Life Science Research (Platform for Drug Discovery, Informatics, and Structural Life Science) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  5. Japan Agency for Medical Research and Development (AMED)
  6. Grants-in-Aid for Scientific Research [15K18833, 15H04634, 24750036] Funding Source: KAKEN

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Disubstituted benzo[b]furans were synthesized by ortho-selective Sonogashira coupling of dichlorophenols and terminal alkynes, followed by cyclization and Suzuki-Miyaura coupling in one pot, using a palladium-dihydroxyterphenylphosphine (Cy-DHTP) catalyst. The use of substoichiometric amounts of tetrabutylammonium chloride was effective in accelerating the Suzuki-Miyaura coupling. This protocol was also successfully applied to the one-pot synthesis of disubstituted indoles from dichloroaniline derivatives.

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