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5-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanenitrile | 1226953-88-3

中文名称
——
中文别名
——
英文名称
5-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanenitrile
英文别名
——
5-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanenitrile化学式
CAS
1226953-88-3
化学式
C12H22BNO3
mdl
——
分子量
239.123
InChiKey
RUWIKPVPBTVHRB-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):
    2.06
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    62.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-酮基已腈联硼酸频那醇酯 在 [1,3-dicyclohexylimidazol-2-yl]copper(I) chloride 、 sodium t-butanolatesilica gel 作用下, 以 甲苯 为溶剂, 反应 6.0h, 以55%的产率得到5-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanenitrile
    参考文献:
    名称:
    Copper-Catalyzed Diboration of Ketones: Facile Synthesis of Tertiary α-Hydroxyboronate Esters
    摘要:
    The diboration of ketones with the (ICy)CuOt-Bu catalyst was developed to provide access to tertiary alpha-hydroxyboronate esters. The (ICy)CuOt-Bu catalyst was generated in situ with (ICy)CuCI and NaOt-Bu to afford a more efficient catalyst than the preformed (ICy)CuOt-Bu. These conditions result in the diboration of various ketones in toluene at 50 degrees C in 2-22 h. Treatment of the resulting products with silica gel affords the corresponding a-hydroxyboronate esters.
    DOI:
    10.1021/ol100468f
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文献信息

  • Copper-Catalyzed Diboration of Ketones: Facile Synthesis of Tertiary α-Hydroxyboronate Esters
    作者:Melissa L. McIntosh、Cameron M. Moore、Timothy B. Clark
    DOI:10.1021/ol100468f
    日期:2010.5.7
    The diboration of ketones with the (ICy)CuOt-Bu catalyst was developed to provide access to tertiary alpha-hydroxyboronate esters. The (ICy)CuOt-Bu catalyst was generated in situ with (ICy)CuCI and NaOt-Bu to afford a more efficient catalyst than the preformed (ICy)CuOt-Bu. These conditions result in the diboration of various ketones in toluene at 50 degrees C in 2-22 h. Treatment of the resulting products with silica gel affords the corresponding a-hydroxyboronate esters.
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