Hydroxycarbonylation of Alkenes with Formic Acid Catalyzed by a Rhodium(III) Hydride Diiodide Complex Bearing a Bidentate Phosphine Ligand

Masaki Okada, Katsuhiko Takeuchi, Kazuhiro Matsumoto, Tomoharu Oku, Takayoshi Yoshimura, Miho Hatanaka, Jun Chul Choi

研究成果: Article査読

抄録

An improved catalytic system was developed for the Rh complex-catalyzed hydroxycarbonylation of alkenes using formic acid (HCOOH). Ligand screening revealed DPEphos, a bidentate phosphine ligand, to be effective, and the corresponding rhodium(III) hydride diiodide complex, RhHI2(CO)(DPEphos) (2), was applied as a catalyst. Complex 2 showed high activity and selectivity in the hydroxycarbonylation of alkenes using HCOOH without any additives and was applicable to a variety of alkene substrates. Analysis of the catalytic cycle using density functional theory calculations was used to elucidate the reaction steps. Initially, an alkyl group was formed by the insertion of an alkene into Rh-H with subsequent acyl group formation via the insertion of a CO ligand, similar to the reaction steps suggested for Rh-catalyzed alkene hydroformylation. The latter part of the catalytic cycle involved the reductive elimination of acyl iodide and subsequent hydrolysis to form a carboxylic acid, analogous to the reaction steps suggested for the synthesis of acetic acid from methanol and CO using a rhodium complex catalyst with hydroiodic acid as an auxiliary catalyst. These results indicate that the iodine atom in complex 2 acts as an auxiliary catalyst during the additive-free hydroxycarbonylation of alkenes using HCOOH.

本文言語English
ページ(範囲)1640-1648
ページ数9
ジャーナルOrganometallics
41
13
DOI
出版ステータスPublished - 2022 7月 11

ASJC Scopus subject areas

  • 物理化学および理論化学
  • 有機化学
  • 無機化学

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