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N-(naphthalen-1-yl)-P,P-diphenylphosphinoselenoic amide | 1384483-02-6

中文名称
——
中文别名
——
英文名称
N-(naphthalen-1-yl)-P,P-diphenylphosphinoselenoic amide
英文别名
(1-NHC10H7)P(Se)Ph2
N-(naphthalen-1-yl)-P,P-diphenylphosphinoselenoic amide化学式
CAS
1384483-02-6
化学式
C22H18NPSe
mdl
——
分子量
406.325
InChiKey
DWQSEFLJEJCGLE-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    N-(naphthalen-1-yl)-1,1-diphenylphosphinamineselenium 作用下, 以 甲苯 为溶剂, 反应 4.0h, 以75%的产率得到N-(naphthalen-1-yl)-P,P-diphenylphosphinoselenoic amide
    参考文献:
    名称:
    Synthesis and Characterization of New N-(Diphenylphosphino)-Naphthylamine Chalcogenides: X-Ray Structures of (1-NHC10H7)P(Se)Ph2 and Ph2P(S)OP(S)Ph2
    摘要:
    The reaction of 1-naphthylamine with one equivalent of chlorodiphenylphosphine in the presence of triethylamine gave the (1-NHC10H7)PPh2 (1) ligand. Refluxing of 1 with elemental sulfur or grey selenium in toluene (1:1 molar ratio) afforded (1-NHC10H7)P(S)Ph-2 (2) and (1-NHC10H7) P(Se) Ph2 (3), respectively. Moreover, the byproduct {Ph2P(S)}(2)O (4) was isolated from the reaction of 1 with elemental sulfur. Compounds 1-3 were identified and characterized by multinuclear (H-1, C-13, P-31, Se-77) NMR spectroscopy, mass spectrometry, and elemental analysis. Crystal structure determinations of 3 and 4 were carried out.
    DOI:
    10.1080/10426507.2012.668985
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