Synthesis of Aryl Phosphines via Pd/C-Catalyzed Decarbonylation of Acylphosphines
C-P bond activation is attractive in the synthesis of trivalent phosphines, but not practical for high requirements in catalyst and reaction conditions. A synthesis of trivalent phosphines via Pd/C-promoted C-P bond activation and decarbonylation of acylphosphines was developed. The reaction was scoped across 31 examples, affording the corresponding trivalent phosphines in yields ranging from 21% to 98%. Pd/C was demonstrated as a more practical and robust catalyst than the previous Ni catalyst because of its higher catalytic activity, recyclability, and tolerance to air and moisture. Further studies on the Pd/C behavior indicated that the Pd/C primarily exerted its catalytic effect through dissolved Pd species, and Pd(II) in Pd/C played a more significant role than Pd(0). This research work not only represented a breakthrough in expanding the applicability of Pd/C catalysts but also marked an advancement in making C-P bond activation reactions more convenient and practical.
Authors
- Minghui Xu (ORCID: https://orcid.org/0000-0001-9567-5569)
- Zhiqian Wang (ORCID: https://orcid.org/0000-0001-9831-649X)
- Wenjuan Mao
- Yuting Zhang
Institutions
- Ingenierie des Materiaux polymeres (FR)
- State Key Laboratory of Chemical Engineering (CN)
- Beijing University of Chemical Technology (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-04-21
- DOI
- https://doi.org/10.1021/acs.joc.6c00348
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Beijing Municipal Natural Science Foundation