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(E)-1-(3-methoxyphenyl)-2-propyl-2-hexen-1-ol | 1610372-05-8

中文名称
——
中文别名
——
英文名称
(E)-1-(3-methoxyphenyl)-2-propyl-2-hexen-1-ol
英文别名
(E)-1-(3-methoxyphenyl)-2-propylhex-2-en-1-ol
(E)-1-(3-methoxyphenyl)-2-propyl-2-hexen-1-ol化学式
CAS
1610372-05-8
化学式
C16H24O2
mdl
——
分子量
248.365
InChiKey
XOHHEGGTULMMAG-UKTHLTGXSA-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):
    4.7
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4-辛炔间甲氧基苯甲醇bis(1,5-cyclooctadiene)nickel (0)1,3-双(2,6-二异丙基苯基)咪唑-2-烯 作用下, 以 为溶剂, 反应 12.0h, 以73%的产率得到(E)-1-(3-methoxyphenyl)-2-propyl-2-hexen-1-ol
    参考文献:
    名称:
    Nickel-Catalyzed Redox-Economical Coupling of Alcohols and Alkynes to Form Allylic Alcohols
    摘要:
    We have developed a redox-economical coupling reaction of alcohols and alkynes to form allylic alcohols under mild conditions. The reaction is redox-neutral as well as redox-economical and thus free from any additives such as a reductant or an oxidant. This atom-economical coupling can be applied for the conversion of both aliphatic and benzylic alcohols to the corresponding substituted allylic alcohols in a single synthetic operation.
    DOI:
    10.1021/ja500666h
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文献信息

  • Nickel-Catalyzed Redox-Economical Coupling of Alcohols and Alkynes to Form Allylic Alcohols
    作者:Kenichiro Nakai、Yuji Yoshida、Takuya Kurahashi、Seijiro Matsubara
    DOI:10.1021/ja500666h
    日期:2014.6.4
    We have developed a redox-economical coupling reaction of alcohols and alkynes to form allylic alcohols under mild conditions. The reaction is redox-neutral as well as redox-economical and thus free from any additives such as a reductant or an oxidant. This atom-economical coupling can be applied for the conversion of both aliphatic and benzylic alcohols to the corresponding substituted allylic alcohols in a single synthetic operation.
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