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2-[(4S,5S)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol | 195731-28-3

中文名称
——
中文别名
——
英文名称
2-[(4S,5S)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol
英文别名
——
2-[(4S,5S)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol化学式
CAS
195731-28-3
化学式
C9H18O4
mdl
——
分子量
190.24
InChiKey
RHSSPMBFYAUHHW-YUMQZZPRSA-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):
    0.27
  • 重原子数:
    13.0
  • 可旋转键数:
    4.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    58.92
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    2-[(4S,5S)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol吡啶正丁基锂甲基磺酰胺 、 AD-mix-β 、 sodium 、 sodium thiosulfate 、 溶剂黄146 、 lithium bromide 作用下, 以 四氢呋喃正己烷二氯甲烷二甲基亚砜 为溶剂, 反应 59.25h, 生成
    参考文献:
    名称:
    Bidirectional and Convergent Routes to oligo(Tetrahydrofurans)
    摘要:
    AbstractOligo(tetrahydrofurans) (oligo‐THFs) 8–12 have been synthesised stereoselectively. Multiple Williamson reactions were used as key steps. While oligo‐THFs with an even number of THF rings like the bi‐THFs 8 and 9 as well as the tetra‐THFs 10 and 11 were obtained by a bidirectional strategy, the penta‐THF 12 with an odd number of THF rings was prepared by a convergent strategy with a sulfone–aldehyde coupling as connecting step. The oligo‐THF products are important structural features of natural (Annonaceae acetogenins) and non‐natural (artificial ion channels) products.
    DOI:
    10.1002/chem.19970030723
  • 作为产物:
    描述:
    [(4S,5S)-2,2-Dimethyl-5-(2-oxo-ethyl)-[1,3]dioxolan-4-yl]-acetaldehyde 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成 2-[(4S,5S)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol
    参考文献:
    名称:
    Bidirectional and Convergent Routes to oligo(Tetrahydrofurans)
    摘要:
    AbstractOligo(tetrahydrofurans) (oligo‐THFs) 8–12 have been synthesised stereoselectively. Multiple Williamson reactions were used as key steps. While oligo‐THFs with an even number of THF rings like the bi‐THFs 8 and 9 as well as the tetra‐THFs 10 and 11 were obtained by a bidirectional strategy, the penta‐THF 12 with an odd number of THF rings was prepared by a convergent strategy with a sulfone–aldehyde coupling as connecting step. The oligo‐THF products are important structural features of natural (Annonaceae acetogenins) and non‐natural (artificial ion channels) products.
    DOI:
    10.1002/chem.19970030723
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