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2,2-Bis(2,3,4,5,6-pentafluorophenyl)-1,4-di(propan-2-yl)-4-aza-1-azonia-2-boranuidacyclopent-5-en-3-one | 1246512-64-0

中文名称
——
中文别名
——
英文名称
2,2-Bis(2,3,4,5,6-pentafluorophenyl)-1,4-di(propan-2-yl)-4-aza-1-azonia-2-boranuidacyclopent-5-en-3-one
英文别名
——
2,2-Bis(2,3,4,5,6-pentafluorophenyl)-1,4-di(propan-2-yl)-4-aza-1-azonia-2-boranuidacyclopent-5-en-3-one化学式
CAS
1246512-64-0
化学式
C20H15BF10N2O
mdl
——
分子量
500.147
InChiKey
YVQAVMTYFVAXIY-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.01
  • 重原子数:
    34
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    23.3
  • 氢给体数:
    0
  • 氢受体数:
    12

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    一氧化碳2,2-Bis(2,3,4,5,6-pentafluorophenyl)-1,3-di(propan-2-yl)-1-aza-3-azonia-2-boranuidacyclobut-3-ene二氯甲烷-D2 为溶剂, 反应 16.0h, 以88%的产率得到2,2-Bis(2,3,4,5,6-pentafluorophenyl)-1,4-di(propan-2-yl)-4-aza-1-azonia-2-boranuidacyclopent-5-en-3-one
    参考文献:
    名称:
    Reactions of Boron Amidinates with CO2 and CO and Other Small Molecules
    摘要:
    Reaction of Piers' borane, HB(C6F5)(2), with either tert-butyl or isopropyl carbodiimide cleanly affords the boron amidinates HC(RN)(2)B(C6F5)(2) [R = iPr (1), tBu (2)]. These species undergo a variety of insertion reactions. For example, treatment of 1 with CO2 or excess carbodiimide gives HC(iPrN)(2)(CO2)B(C6F5)(2) (3) or HC(iPrN)(2)C(iPrN)(2)B(C6F5)(2) (4), respectively. Similarly, exposure of 1 or 2 to 1 atm CO gives HC(RN)(2)(CO)B(C6F5)(2) [R = iPr (5), tBu (6)], while reaction of 1 with CNtBu gives HC(RN)(2)(CNtBu)B(C6F5)(2) [R = iPr (7), tBu (8)]. Compounds 1 and 2 also react with benzaldehyde, resulting in the formation of HC(RN)(2)(PhHCO)B(C6F5)(2) [R = iPr (9), tBu (10)]. Compound 1 also reacts with MeCN to give HC(iPrN)(2)-(MeCN)B(C6F5)(2) (11) and effects heterolytic C H cleavage to afford HC(iPrN)(iPrNH)(PhCC)B(C6F5)(2) (12). In contrast, the species PhC(iPrN)(2)B(C6F5)(2) (14) derived from PhC(iPrN)(2)BCl2 (13) failed to react with any of the above substrates. These data, in addition to the isolation of HC(iPrN)(2)(C6F4)BF(C6F5) (15), the product of thermolysis of 1, provide further support for the notion that the transient "open-chain" form of these amidinates is present in solution.
    DOI:
    10.1021/ja1064153
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