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Merck
CN
  • Synthesis of dibenzofurans directly from aryl halides and ortho-bromophenols via one-pot consecutive SNAr and intramolecular palladium-catalyzed aryl-aryl coupling reactions.

Synthesis of dibenzofurans directly from aryl halides and ortho-bromophenols via one-pot consecutive SNAr and intramolecular palladium-catalyzed aryl-aryl coupling reactions.

Chemical & pharmaceutical bulletin (2008-10-02)
Hui Xu, Ling-Ling Fan
摘要

A series of dibenzofurans were efficiently and conveniently synthesized via one-pot consecutive C(sp(2))-O bond formation reaction (SNAr) in the presence of anhydrous K(2)CO(3), followed by C(sp(2))-C(sp(2)) bond formation reaction (intramolecular palladium-catalyzed aryl-aryl coupling reaction) between aryl halides and ortho-bromophenols. The desired dibenzofurans were obtained in 32-99% isolated yields.

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Sigma-Aldrich
铬酸钾, ACS reagent, ≥99.0%
Sigma-Aldrich
铬酸钾, puriss., ≥99%
Sigma-Aldrich
2-溴苯酚, 98%
Sigma-Aldrich
铬酸钾, ≥99.95% trace metals basis