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1-(2-Methyl-1-((tri-n-butylsilyl)methyl)-2-propenyl)cyclohexanol | 133448-00-7

中文名称
——
中文别名
——
英文名称
1-(2-Methyl-1-((tri-n-butylsilyl)methyl)-2-propenyl)cyclohexanol
英文别名
1-(2-Methyl-I-tri(n-butyl)silylmethyl-2-propenyl)cyclohexanol;1-(3-methyl-1-tributylsilylbut-3-en-2-yl)cyclohexan-1-ol
1-(2-Methyl-1-((tri-n-butylsilyl)methyl)-2-propenyl)cyclohexanol化学式
CAS
133448-00-7
化学式
C23H46OSi
mdl
——
分子量
366.703
InChiKey
GAQFVVFMTZIZRA-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

物化性质

  • 沸点:
    430.3±20.0 °C(Predicted)
  • 密度:
    0.882±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.72
  • 重原子数:
    25
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-(2-Methyl-1-((tri-n-butylsilyl)methyl)-2-propenyl)cyclohexanol 、 1-(1-methyl-1-((tri-n-butylsilyl)-methyl)-2-propenyl)cyclohexanol 、 、 、 、 、 、 、 1-(2-(4-Methyl-3-pentenyl)-1-((trimethylsilyl)methyl)-2-propenyl)cyclohexanol 、 1-(1-ethenyl-5-methyl-1-((trimethylsilyl)methyl)-4-hexenyl)cyclohexanol 、 、 、 、 、 以 为溶剂, 生成 2,7-Diphenyl-5-silaspiro<4.4>nona-2,7-diene
    参考文献:
    名称:
    Preparation and use of (2-butene-1,4-diyl)magnesium complexes in organic
    摘要:
    环烃的镁配合物,比如1,2-二亚甲基环烷烃,可以使用高反应性的镁轻易制备得到高收率。这些(2-丁烯-1,4-二基)镁试剂与电子亲和剂,如二溴代烷、烷基重甲基苯磺酸酯或溴代烷基腈的反应,可作为合成螺环系统的方便方法。值得注意的是,通过这种方法制备的螺环碳环化合物是在由国家卫生研究院授予的GM35153合同支持下完成的。政府对该发明有一定的权利。
    公开号:
    US05231205A1
  • 作为产物:
    描述:
    三丁基氯硅烷环己酮天然橡胶magnesium 作用下, 生成 1-(1-methyl-1-((tri-n-butylsilyl)-methyl)-2-propenyl)cyclohexanol 、 1-(2-Methyl-1-((tri-n-butylsilyl)methyl)-2-propenyl)cyclohexanol
    参考文献:
    名称:
    Chemistry of substituted (2-butene-1,4-diyl)magnesium: a facile approach to complex carbocycles, functionalized ketones and alcohols, and silicon-containing heterocycles
    摘要:
    Highly reactive magnesium reacts with a wide variety of substituted 1,3-dienes to give the corresponding substituted (2-butene-1,4-diyl)magnesium complexes. Reactions of symmetrical (2-butene-1,4-diyl)magnesium with alpha,omega-alkylene dihalides form three-, four-, five-, and six-membered carbocycles. Significantly, the cyclizations are always stereospecific and completely regioselective. Depending on the initial 1,3-diene and specific electrophiles, uncyclized products can be obtained. Stepwise reactions of (2,3-dimethyl-2-butene-1,4-diyl)magnesium with two different electrophiles afford polyfunctionalized ketones with the generation of a quaternary center. Formal 1,2-additions can be effected in this manner. Substituted five- and six-membered cyclic ketones can also be synthesized in one step by this approach. Treatment of unsymmetrical (2-butene-1,4-diyl)magnesium complexes with triorganosilyl chlorides followed by cyclohexanone results in additions across a terminal double bond with high regioselectivity. Silicon-containing heterocycles or spiro compounds can be readily synthesized by using the bis-Grignard reagents.
    DOI:
    10.1021/jo00009a034
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文献信息

  • Chemistry of substituted (2-butene-1,4-diyl)magnesium: a facile approach to complex carbocycles, functionalized ketones and alcohols, and silicon-containing heterocycles
    作者:Reuben D. Rieke、Heping Xiong
    DOI:10.1021/jo00009a034
    日期:1991.4
    Highly reactive magnesium reacts with a wide variety of substituted 1,3-dienes to give the corresponding substituted (2-butene-1,4-diyl)magnesium complexes. Reactions of symmetrical (2-butene-1,4-diyl)magnesium with alpha,omega-alkylene dihalides form three-, four-, five-, and six-membered carbocycles. Significantly, the cyclizations are always stereospecific and completely regioselective. Depending on the initial 1,3-diene and specific electrophiles, uncyclized products can be obtained. Stepwise reactions of (2,3-dimethyl-2-butene-1,4-diyl)magnesium with two different electrophiles afford polyfunctionalized ketones with the generation of a quaternary center. Formal 1,2-additions can be effected in this manner. Substituted five- and six-membered cyclic ketones can also be synthesized in one step by this approach. Treatment of unsymmetrical (2-butene-1,4-diyl)magnesium complexes with triorganosilyl chlorides followed by cyclohexanone results in additions across a terminal double bond with high regioselectivity. Silicon-containing heterocycles or spiro compounds can be readily synthesized by using the bis-Grignard reagents.
  • Preparation and use of (2-butene-1,4-diyl)magnesium complexes in organic
    申请人:Board of Regents of the University of Nebraska
    公开号:US05231205A1
    公开(公告)日:1993-07-27
    The magnesium complexes of cyclic hydrocarbons, such as 1,2-dimethylenecycloalkanes, are readily prepared in high yields using highly reactive magnesium. Reactions of these (2-butene-1,4-diyl)magnesium reagents with electrophiles such as dibromoalkanes, alkylditosylates, or bromoalkylnitriles serve as a convenient method for synthesizing spirocyclic systems. Significantly, spirocarbocycles prepared by this The present invention was made with Government support under Contract No. GM35153 awarded by the National Institute of Health. The Government has certain rights in the invention.
    环烃的镁配合物,比如1,2-二亚甲基环烷烃,可以使用高反应性的镁轻易制备得到高收率。这些(2-丁烯-1,4-二基)镁试剂与电子亲和剂,如二溴代烷、烷基重甲基苯磺酸酯或溴代烷基腈的反应,可作为合成螺环系统的方便方法。值得注意的是,通过这种方法制备的螺环碳环化合物是在由国家卫生研究院授予的GM35153合同支持下完成的。政府对该发明有一定的权利。
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