Dicyclohexyl-(3-phenylpropyl)phosphine | 222055-10-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: Dicyclohexyl-(3-phenylpropyl)phosphine
• 英文别名: dicyclohexyl(3-phenylpropyl)phosphine；(3-Phenylpropyl) dicyclohexyl-phosphine；dicyclohexyl(3-phenylpropyl)phosphane
• CAS: 222055-10-9
• 化学式: C₂₁H₃₃P
• 分子量: 316.467
• InChiKey: FELJPQLGGRIRHR-UHFFFAOYSA-N

物化性质

• 沸点：
  434.9±15.0 °C(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  22
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂ 、 Dicyclohexyl-(3-phenylpropyl)phosphine 以 二氯甲烷 为溶剂， 以84%的产率得到[RuCl2(p-cymene)(dicyclohexyl(3-phenylpropyl)phosphine)]
  参考文献：
  名称：

  Synthesis and evaluation of new RuCl2(p-cymene)(ER2R′) and (η1:η6-phosphinoarene)RuCl2 complexes as ring-opening metathesis polymerization catalysts

  摘要：

  New RuCl2(p-cymene)(ER2R') complexes (E = P, As, Sb; R, R' = H, alkyl, arylalkyl) have been synthesized and used as catalyst precursors for the ring-opening metathesis polymerization (ROMP) of cyclooctene, cyclopentene, and norbornene. When ER2R' was a phosphinoarene, the p-cymene ligand could be displaced upon heating and tethered (eta(1):eta(6)-phosphinoarene)RuCl2 complexes were obtained. Simple thermogravimetric analysis (TGA) of the complexes provided clear-cut indication on their potential catalytic activity in ROMP. (C) 2000 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0022-328x(00)00287-4
• 作为产物：
  描述：

  二环己基氯化膦 在 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 、 正戊烷 为溶剂， 反应 18.0h， 生成 Dicyclohexyl-(3-phenylpropyl)phosphine
  参考文献：
  名称：

  Synthesis and evaluation of new RuCl2(p-cymene)(ER2R′) and (η1:η6-phosphinoarene)RuCl2 complexes as ring-opening metathesis polymerization catalysts

  摘要：

  New RuCl2(p-cymene)(ER2R') complexes (E = P, As, Sb; R, R' = H, alkyl, arylalkyl) have been synthesized and used as catalyst precursors for the ring-opening metathesis polymerization (ROMP) of cyclooctene, cyclopentene, and norbornene. When ER2R' was a phosphinoarene, the p-cymene ligand could be displaced upon heating and tethered (eta(1):eta(6)-phosphinoarene)RuCl2 complexes were obtained. Simple thermogravimetric analysis (TGA) of the complexes provided clear-cut indication on their potential catalytic activity in ROMP. (C) 2000 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0022-328x(00)00287-4

文献信息

• CsOH-promoted P-alkylation: a convenient and highly efficient synthesis of tertiary phosphines
  作者：Matthew T Honaker、Benjamin J Sandefur、James L Hargett、Alicia L McDaniel、Ralph Nicholas Salvatore

  DOI：10.1016/j.tetlet.2003.09.117

  日期：2003.11

  and efficient method for the synthesis of tertiary phosphines and ditertiary phosphines has been developed. In the presence of cesium hydroxide, molecular sieves and DMF at room temperature, various secondary phosphines and alkyl bromides were examined, and the results have demonstrated that this methodology offers a general synthetic procedure to produce tertiary phosphines in moderate to high yields

  已经开发了温和而有效的合成叔膦和二叔膦的方法。在室温下存在氢氧化铯，分子筛和DMF的情况下，检查了各种仲膦和烷基溴化物，结果表明，该方法可提供一般的合成方法，以中等至高收率生产叔膦。还描述了旋光性叔膦的合成。
• Fuerstner, Alois; Liebl, Monika; Lehmann, Christian W., Chemistry - A European Journal, 2000, vol. 6, # 10, p. 1847 - 1857
  作者：Fuerstner, Alois、Liebl, Monika、Lehmann, Christian W.、Picquet, Michel、Kunz, Rainer、Bruneau, Christian、Touchard, Daniel、Dixneuf, Pierre H.

  DOI：——

  日期：——