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[Me2Al(μ-tetrahydrofurfuryl)]2 | 847466-10-8

中文名称
——
中文别名
——
英文名称
[Me2Al(μ-tetrahydrofurfuryl)]2
英文别名
——
[Me2Al(μ-tetrahydrofurfuryl)]2化学式
CAS
847466-10-8;847622-99-5
化学式
C14H30Al2O4
mdl
——
分子量
316.353
InChiKey
SUHIFFFEMNZRHP-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    2,6-二甲基苯酚[Me2Al(μ-tetrahydrofurfuryl)]2甲苯 为溶剂, 以77.7%的产率得到[Al(Me)(OC6H3(Me)2-2,6)(μ-tetrahydrofurfuryl)]2
    参考文献:
    名称:
    Tetrahydrofurfuryloxide Derivatives of Alkyl Aluminum Species
    摘要:
    Tetrahydrofurfuryl alcohol (H-OTHF) was successfully reacted with a series of aluminum alkyls (AlR3) to yield compounds of the general formula [R2Al(mu-OTHF)](2) where R = CH3 (1), CH2CH3 (2), and CH2CH(CH3)2 (3). Further, reactivity studies showed that the alkyls for 1 were easily exchanged, forming compounds of the general formula [Me(OR)Al(mu-OTHF)](2) where OR = OC6H3(Me)(2)-2,6 (4), OC6H3(CMe3)(2)-2,6 (5a), and OSi(C6H5)(3) (6). For 5a, reflux temperatures were required to get the full exchange; otherwise the asymmetric derivative [Me(OR)Al(mu-OTHF)(2)AlMe2] (5b) was isolated. The bulk powders of 1-6 were found to be in agreement with the crystal structures on the basis of elemental analyses and multinuclear solid state NMR studies. Multinuclear solution state NMR studies indicate that the alkyl OTHF derivatives have cis/trans isomers due to the chiral proton on the OTHF ligand.
    DOI:
    10.1021/om0493199
  • 作为产物:
    描述:
    四氢糠醇三甲基铝甲苯 为溶剂, 以88.1%的产率得到[Me2Al(μ-tetrahydrofurfuryl)]2
    参考文献:
    名称:
    Tetrahydrofurfuryloxide Derivatives of Alkyl Aluminum Species
    摘要:
    Tetrahydrofurfuryl alcohol (H-OTHF) was successfully reacted with a series of aluminum alkyls (AlR3) to yield compounds of the general formula [R2Al(mu-OTHF)](2) where R = CH3 (1), CH2CH3 (2), and CH2CH(CH3)2 (3). Further, reactivity studies showed that the alkyls for 1 were easily exchanged, forming compounds of the general formula [Me(OR)Al(mu-OTHF)](2) where OR = OC6H3(Me)(2)-2,6 (4), OC6H3(CMe3)(2)-2,6 (5a), and OSi(C6H5)(3) (6). For 5a, reflux temperatures were required to get the full exchange; otherwise the asymmetric derivative [Me(OR)Al(mu-OTHF)(2)AlMe2] (5b) was isolated. The bulk powders of 1-6 were found to be in agreement with the crystal structures on the basis of elemental analyses and multinuclear solid state NMR studies. Multinuclear solution state NMR studies indicate that the alkyl OTHF derivatives have cis/trans isomers due to the chiral proton on the OTHF ligand.
    DOI:
    10.1021/om0493199
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