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3-methoxy-5-(4-methylpent-3-enyl)pyridine | 1159426-50-2

中文名称
——
中文别名
——
英文名称
3-methoxy-5-(4-methylpent-3-enyl)pyridine
英文别名
3-Methoxy-5-(4-methylpent-3-enyl)pyridine
3-methoxy-5-(4-methylpent-3-enyl)pyridine化学式
CAS
1159426-50-2
化学式
C12H17NO
mdl
——
分子量
191.273
InChiKey
WCERDLFSFABVBM-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):
    3
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-溴-5-甲氧基吡啶 、 在 potassium fluoride 、 palladium diacetate 、 potassium carbonate2-二环己基磷-2,4,6-三异丙基联苯2-二环己基磷-2',6'-二异丙氧基-1,1'-联苯 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以33.2 mg的产率得到3-methoxy-5-(4-methylpent-3-enyl)pyridine
    参考文献:
    名称:
    Utilization of Potassium Vinyltrifluoroborate in the Development of a 1,2-Dianion Equivalent
    摘要:
    Previous studies of orthogonally reactive dibora species led to the discovery of a unique reactivity pattern associated with potassium vinyltrifluoroborate. Upon hydroboration, the vinyltrifluoroborate generates a 1,2-diboraethane, which is distinct from the 1,1-dibora intermediates generated when traditional alkenyldialkylboron species undergo hydroboration. The 1,2-dianion equivalent thus generated can be envisioned as a building block for the linkage of two different electrophiles via palladium-catalyzed Suzuki-Miyaura cross-couplings.
    DOI:
    10.1021/ol900822j
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文献信息

  • Utilization of Potassium Vinyltrifluoroborate in the Development of a 1,2-Dianion Equivalent
    作者:Gary A. Molander、Deidre L. Sandrock
    DOI:10.1021/ol900822j
    日期:2009.6.4
    Previous studies of orthogonally reactive dibora species led to the discovery of a unique reactivity pattern associated with potassium vinyltrifluoroborate. Upon hydroboration, the vinyltrifluoroborate generates a 1,2-diboraethane, which is distinct from the 1,1-dibora intermediates generated when traditional alkenyldialkylboron species undergo hydroboration. The 1,2-dianion equivalent thus generated can be envisioned as a building block for the linkage of two different electrophiles via palladium-catalyzed Suzuki-Miyaura cross-couplings.
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