1,2-dicyclohexyldiborane(6) | 41757-52-2

• 英文名称: 1,2-dicyclohexyldiborane(6)
• 英文别名: 1,2-dicyclohexyldiborane；cyclohexylborane dimer
• CAS: 41757-52-2
• 化学式: C₁₂H₂₆B₂
• 分子量: 191.96
• InChiKey: KHEZIKLXGWKWHL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  1,2-dicyclohexyldiborane(6) 在 吡啶 作用下， 生成 1,2-dicyclohexyldiborane(6)*pyridine
  参考文献：
  名称：

  Simple general synthesis of monoalkylboranes and their applicability for the preparation of mixed organoboranes via hydroboration

  摘要：

  DOI：

  10.1021/ja00745a049
• 作为产物：
  描述：

  三乙基硅烷 、 (二氯)(环己基)硼烷 以 neat (no solvent) 为溶剂， 生成 1,2-dicyclohexyldiborane(6)
  参考文献：
  名称：

  卤硼烷/三烷基硅烷混合物进行硼氢化

  摘要：

  Trialkylsilanes or dialkylsilanes react rapidly with boron trichloride in the absence of ethereal solvents or other nucleophiles to form unsolvated dichloroborane. If no substrate is present, dichloroborane disproportionates to trichloroborane and two geometric isomers of chloroborane dimer, which in turn yield monochlorodiborane and, slowly but irreversibly, diborane. All of the B-H compounds in the mixture except diborane are highly active hydroborating agents. With alkenes in the presence of sufficient boron trichloride, the products are alkyldichloroboranes. These are free from detectable contamination by dialkylchloroboranes unless more than 1 mol of hydride is present. Similar hydroboration of terminal acetylenes can be controlled to yield either (E)-1-(dichloroboryl)alkenes or 1,1-bis(dichloroboryl)alkanes, each free from significant contamination by the other. Alkyldichloroboranes with trialkylsilanes at 25 degrees C produce alkylmonochloroboranes, detected by B-11 NMR. 1,1-Bis(dichloroboryl)alkanes similarly yield 1,1-diborylalkane dimers. An alkylmonochloroborane can hydroborate a second alkene to form a dialkylchloroborane. For this purpose, differing alkyl groups may be introduced in either order, regardless of their relative steric properties. With 2 mol of trialkylsilane, alkyldichloroboranes are converted to alkylborane dimers. Boron tribromide and its bromoborane derivatives behave similarly to the chloro compounds in the examples tested.

  DOI：

  10.1021/om00009a018

文献信息

• Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: B: B-Verb.14, 5, page 201 - 212
  作者：

  DOI：——

  日期：——