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1,4-Bismethylenespiropentane | 56955-52-3

中文名称
——
中文别名
——
英文名称
1,4-Bismethylenespiropentane
英文别名
rac-1,4-dimethylenespiropentane;2,5-Dimethylidenespiro[2.2]pentane
1,4-Bismethylenespiropentane化学式
CAS
56955-52-3
化学式
C7H8
mdl
——
分子量
92.1405
InChiKey
PJLIDZOYPXCQIT-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:
    106.2±10.0 °C(Predicted)
  • 密度:
    0.94±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 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:
    1,4-Dichloro-1,4-dimethylspiropentane 在 potassium tert-butylate 作用下, 以 二甲基亚砜 为溶剂, 以20%的产率得到1,4-Bismethylenespiropentane
    参考文献:
    名称:
    The synthesis of bismethylene derivatives of triangulanes
    摘要:
    A method for the preparation of an unique type of hyrocarbons, namely, bismethylene derivatives of linear triangulanes, has been developed, and the syntheses of 1,4-bismethylenespiropentane, 1,5-bismethylenedispiro[2.0.2.1]heptanes, and 1,6-bismethylenetrispiro[2.0.0.2.1.1]nonanes were realized.
    DOI:
    10.1016/s0040-4020(01)86528-5
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文献信息

  • The First Enantiomerically Pure [n]Triangulanes and Analogues: σ-[n]Helicenes with Remarkable Features
    作者:Armin de Meijere、Alexander F. Khlebnikov、Sergei I. Kozhushkov、Rafael R. Kostikov、Peter R. Schreiner、Alexander Wittkopp、Christopher Rinderspacher、Henning Menzel、Dmitrii S. Yufit、Judith A. K. Howard
    DOI:10.1002/1521-3765(20020215)8:4<828::aid-chem828>3.0.co;2-y
    日期:2002.2.15
    (M)-(-)- and (P)-(+)-Thspiro-[2.0.0.2.1.1]nonanes [(M)- and (P)-3] as well as (M)-(-)- and (P)-(+)-tetraspiro[2.0.0.0.2.1.1.1]undecanes [(M)- and (P)4]-enantiomerically pure unbranched [4]- and [5]triangulanes-have been prepared starting from racemic bicyclopropylidenecarboxylic [(1RS)-12] and exo-dispiro[2.0.2.1]heptane-1-carboxylic [(lRS,3SR)-13] acids. The optical resolutions of rac-12 and rac-13 furnished enantiomerically pure acids (S)-(+)12, (R)-(-)-12, (1R,3S)-(-)-13, and (1S,3R)-(+)-13. The ethyl ester (R)-25 of the acid (R)-(-)-12 was cyclopropanated to give carboxylates (1R,3R)-26 and (1R,3S)-26. The ester (IR,3S)-26 and acids (1R,3S)-13 and (IS,3R)-13 were converted into enantiomerically pure methylene[3]triangulanes (S)-(-)and (R)-(+)-28. An alternative approach consisted of an enzymatic deracemization of endo-[(1SR,3SR)-dispiro[2.0.2. 1]heptyl] methanol (rac-20) or anti- [(1SR.3RS)-4-methylenespiropentyl]methanol (rac-18). This afforded (S)-(-)- and (R)-(+)-28 (starting from rac-20), as well as enantiomerically pure (M)-(-)- and (P)-(+)-l,4-dimethylenespiropentanes [(M)- and (P)-23] starting from rac-18. The methylenetriangulanes (S)-(-)- and (R)-(+)-28 were cyclopropanated furnishing (M)- and (P)-3. The rhodium-catalyzed cycloaddition of ethyl diazoacetate onto (S)-(-)- and (R)(+)-28 yielded four diastereomeric ethyl trispiro[2.0.0.2.1.1]nonane-1-carboxylates in approximately equal proportions. The enantiomerically pure esters (1R,3S,4S)- and (1S,3R,4R)-30 were isolated by careful distillation and then transformed into [5]triangulanes (M)and (P)-4 using the same sequence of reactions Lis applied for (M)- and (P)-3. The structures of the key intermediates (R)-12 and rac-31 were confirmed by X-ray analyses. Although [4]- and [5]triangulanes have no chromophore which would lead to any significant absorption above 200 nm. they have remarkably high specific rotations even at 589 nm with [alpha](20)(1)) = -192.7 [(M)-3, c=1.18, CHCl3)] or + 373.0 [(P)-4, c=1.18, CHCl3]. This remarkable optical rotatation is in line with their helical arrangement of sigma bonds, as confirmed by a full valence space single excitation configuration interaction treatment (SCI) in conjunction with DFT computations at the B3LYP/TZVP//B3LYP/6-31 +G(d,p) level of theory which reproduce the ORD very well. Thus, it is appropriate to call the helically shaped unbranched [n]triangulanes the "sigma-[n]helicenes", representing the sigma-bond analogues of the aromatic [n]helicenes.
  • The synthesis of bismethylene derivatives of triangulanes
    作者:Kirill A Lukin、Anna Yu Masunova、Bogdan I Ugrak、Nikolai S Zefirov
    DOI:10.1016/s0040-4020(01)86528-5
    日期:1991.7
    A method for the preparation of an unique type of hyrocarbons, namely, bismethylene derivatives of linear triangulanes, has been developed, and the syntheses of 1,4-bismethylenespiropentane, 1,5-bismethylenedispiro[2.0.2.1]heptanes, and 1,6-bismethylenetrispiro[2.0.0.2.1.1]nonanes were realized.
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