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2,3-dibenzylbut-1-ene

中文名称
——
中文别名
——
英文名称
2,3-dibenzylbut-1-ene
英文别名
(3-Benzyl-2-methylbut-3-enyl)benzene
2,3-dibenzylbut-1-ene化学式
CAS
——
化学式
C18H20
mdl
——
分子量
236.357
InChiKey
XGJKHBLRRVKYMP-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):
    5.8
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    烯丙苯氯化二乙基铝bis(acetylacetonate)nickel(II)二氯二茂锆 magnesium3-氯丙烯 作用下, 生成 trans-1,2-dibenzylcyclopentane 、 2,3-dibenzylbut-1-ene
    参考文献:
    名称:
    Synthesis and transformations of metallocycles
    摘要:
    A novel regio- and stereoselective method for synthesizing threo-2,3-disubstituted 1,4-dialumobutanes from alpha-olefins and haloalanes (Et(2)AlCl, (Et(2)N)(2)AlCl, (EtO)(2)AlCl, Bu(2)(i)AlCl) with the participation of catalytic amounts of Cp(2)ZrCl(2) or ZrCl4 in the presence of magnesium metal was developed. The products of hydrolysis and deuterolysis of the dialuminum compounds obtained have a threo-configuration. The selective transformations of 1,4-dialumobutanes to trans-3,4-disubstituted tetrahydrothiophenes, trans-1,2-disubstituted cyclobutanes, and disubstituted alpha,omega-dienes were found to be possible.
    DOI:
    10.1007/bf00714441
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文献信息

  • Synthesis and transformations of metallocycles
    作者:U. M. Dzhemilev、A. G. Ibragimov、V. N. Azhgaliev、R. R. Muslukhov
    DOI:10.1007/bf00714441
    日期:1995.8
    A novel regio- and stereoselective method for synthesizing threo-2,3-disubstituted 1,4-dialumobutanes from alpha-olefins and haloalanes (Et(2)AlCl, (Et(2)N)(2)AlCl, (EtO)(2)AlCl, Bu(2)(i)AlCl) with the participation of catalytic amounts of Cp(2)ZrCl(2) or ZrCl4 in the presence of magnesium metal was developed. The products of hydrolysis and deuterolysis of the dialuminum compounds obtained have a threo-configuration. The selective transformations of 1,4-dialumobutanes to trans-3,4-disubstituted tetrahydrothiophenes, trans-1,2-disubstituted cyclobutanes, and disubstituted alpha,omega-dienes were found to be possible.
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