4.7 Article

Convenient synthesis of phosphinecarboxamide and phosphinecarbothioamide by hydrophosphination of isocyanates and isothiocyanates

Journal

CHEMICAL COMMUNICATIONS
Volume 56, Issue 3, Pages 443-445

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc08329d

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Funding

  1. JSPS [16K05728]
  2. JSPS, Japan [15H00957]
  3. Grants-in-Aid for Scientific Research [15H00957, 16K05728] Funding Source: KAKEN

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Reactions of isocyanates with primary and secondary phosphines without solvent at room temperature afforded the corresponding phosphinecarboxamide (RN(H)COPR '(2)) in excellent yields. This reaction system is applicable for isothiocyanates. The compounds newly obtained were fully characterized using multielement NMR spectroscopy. In addition, the molecular structure of Cl(CH2)(2)N(H)COPPh2 was studied by single-crystal X-ray diffraction.

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