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4-ethyl-2-hexyl-2-methyl-1,3-dioxolane

中文名称
——
中文别名
——
英文名称
4-ethyl-2-hexyl-2-methyl-1,3-dioxolane
英文别名
——
4-ethyl-2-hexyl-2-methyl-1,3-dioxolane化学式
CAS
——
化学式
C12H24O2
mdl
——
分子量
200.321
InChiKey
OMNMFXDKFCPMPZ-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):
    3.9
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-辛炔1,2-丁二醇 在 [Ir(1,5-cyclooctadiene)2]PF6 三异丙基亚磷酸酯氯化锆(IV) 作用下, 以 1,4-二氧六环 为溶剂, 反应 15.0h, 以86%的产率得到4-ethyl-2-hexyl-2-methyl-1,3-dioxolane
    参考文献:
    名称:
    Iridium complex-catalyzed addition of water and alcohols to non-activated terminal alkynes
    摘要:
    The addition of water and alcohols to non-activated terminal alkynes was found to be promoted by an iridium complex combined with Lewis acid and phosphite. Thus, terminal alkynes reacted with water or alcohols to give ketones or ketals, respectively, in good to excellent yields. alpha,omega-Diyne like 1,7-octadiyne, was converted into 1-(2-methyl-cyclopent-1-enyl)ethanone through the intramoleculer aldol condensation of the resulting 2,7-octanedione induced by Lewis acid. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.12.010
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文献信息

  • Iridium complex-catalyzed addition of water and alcohols to non-activated terminal alkynes
    作者:Tomotaka Hirabayashi、Yoshio Okimoto、Akiyo Saito、Masao Morita、Satoshi Sakaguchi、Yasutaka Ishii
    DOI:10.1016/j.tet.2005.12.010
    日期:2006.3
    The addition of water and alcohols to non-activated terminal alkynes was found to be promoted by an iridium complex combined with Lewis acid and phosphite. Thus, terminal alkynes reacted with water or alcohols to give ketones or ketals, respectively, in good to excellent yields. alpha,omega-Diyne like 1,7-octadiyne, was converted into 1-(2-methyl-cyclopent-1-enyl)ethanone through the intramoleculer aldol condensation of the resulting 2,7-octanedione induced by Lewis acid. (c) 2005 Elsevier Ltd. All rights reserved.
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