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methyl 3,5-bis(undec-10-yn-1-yloxy)benzoate | 1346557-03-6

中文名称
——
中文别名
——
英文名称
methyl 3,5-bis(undec-10-yn-1-yloxy)benzoate
英文别名
Methyl 3,5-bis(undec-10-ynoxy)benzoate;methyl 3,5-bis(undec-10-ynoxy)benzoate
methyl 3,5-bis(undec-10-yn-1-yloxy)benzoate化学式
CAS
1346557-03-6
化学式
C30H44O4
mdl
——
分子量
468.677
InChiKey
CPEHDIPUVVFEBL-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):
    9.7
  • 重原子数:
    34
  • 可旋转键数:
    22
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 3,5-bis(undec-10-yn-1-yloxy)benzoate吡啶氧气三乙胺 、 nickel(II) nitrate 、 copper dichloride 作用下, 以 甲醇 为溶剂, 以69%的产率得到
    参考文献:
    名称:
    Phase Separation As a Strategy Toward Controlling Dilution Effects in Macrocyclic Glaser-Hay Couplings
    摘要:
    Macrocycles are abundant in numerous chemical applications, however the traditional strategy for the preparation of these compounds remains cumbersome and environmentally damaging; involving tedious reaction set-ups and extremely dilute reaction media. The development of a macrocyclization strategy conducted at high concentrations is described which exploits phase separation of the catalyst and substrate, as a strategy to control dilution effects. Sequestering a copper catalyst in a highly polar and/or hydrophilic phase can be achieved using a hydrophilic ligand, T-PEG(1900), a PEGylated TMEDA derivative. Similarly, phase separation is possible when suitable copper complexes are soluble in PEG(400), a green and efficient solvent which can be utilized in biphasic mixtures for promoting macrocyclization at high concentrations. The latter phase separation technique can be exploited for the synthesis of a wide range of industrially relevant macrocycles with varying ring sizes and functional groups.
    DOI:
    10.1021/ja208902t
  • 作为产物:
    描述:
    10-十一碳炔酸 在 lithium aluminium tetrahydride 、 偶氮二甲酸二异丙酯三苯基膦 作用下, 以 四氢呋喃 为溶剂, 反应 30.0h, 生成 methyl 3,5-bis(undec-10-yn-1-yloxy)benzoate
    参考文献:
    名称:
    Phase Separation As a Strategy Toward Controlling Dilution Effects in Macrocyclic Glaser-Hay Couplings
    摘要:
    Macrocycles are abundant in numerous chemical applications, however the traditional strategy for the preparation of these compounds remains cumbersome and environmentally damaging; involving tedious reaction set-ups and extremely dilute reaction media. The development of a macrocyclization strategy conducted at high concentrations is described which exploits phase separation of the catalyst and substrate, as a strategy to control dilution effects. Sequestering a copper catalyst in a highly polar and/or hydrophilic phase can be achieved using a hydrophilic ligand, T-PEG(1900), a PEGylated TMEDA derivative. Similarly, phase separation is possible when suitable copper complexes are soluble in PEG(400), a green and efficient solvent which can be utilized in biphasic mixtures for promoting macrocyclization at high concentrations. The latter phase separation technique can be exploited for the synthesis of a wide range of industrially relevant macrocycles with varying ring sizes and functional groups.
    DOI:
    10.1021/ja208902t
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文献信息

  • Continuous flow macrocyclization at high concentrations: synthesis of macrocyclic lipids
    作者:Anne-Catherine Bédard、Sophie Régnier、Shawn K. Collins
    DOI:10.1039/c3gc40872h
    日期:——
    A phase separation/continuous flow macrocyclization protocol eliminates the need for high-dilution conditions and can be used to prepare gram quantities of biologically relevant macrocyclic lipid structures. The method presents several green advantages towards macrocycle synthesis: (1) the prevention of unwanted oligomers and waste, (2) a reduction in the large quantities of toxic, volatile organic solvents and (3) the use of PEG as an environmentally benign reaction media. Macrocycles could be synthesized in high yields (up to 99%) in short reaction times (1.5 h) and on gram scales without the need to alter the reaction conditions.
    相分离/连续流大环化方案无需高稀释条件,可用于制备克级数量的生物相关大环脂质结构。该方法在大环合成方面具有多项绿色优势:(1) 避免了不必要的低聚物和废物;(2) 减少了大量有毒、易挥发的有机溶剂;(3) 使用 PEG 作为对环境无害的反应介质。大环化合物的合成收率高(高达 99%),反应时间短(1.5 小时),以克为单位,无需改变反应条件。
  • Exploiting Aggregation To Achieve Phase Separation in Macrocyclization
    作者:Anne-Catherine Bédard、Shawn K. Collins
    DOI:10.1002/chem.201203433
    日期:2013.2.4
    The aggregation properties of poly(ethylene glycol) (PEG) can be exploited in organic synthesis to control dilution effects. Through the use of solvent mixtures containing PEG400/MeOH, macrocyclization by Glaser–Hay coupling can be conducted at high concentrations. The origin of the selectivity has been studied by using surface tension measurements, UV spectroscopy, and chemical tagging and demonstrates
    可以在有机合成中利用聚乙二醇(PEG)的聚集特性来控制稀释效果。通过使用包含PEG 400 / MeOH的溶剂混合物,可以在高浓度下通过Glaser-Hay偶联进行大环化。通过使用表面张力测量,紫外光谱和化学标记研究了选择性的起源,并证明了收率和选择性对PEG 400聚集的依赖性及其优先溶解有机底物的能力,从而导致了相分离。催化剂体系。
  • Phase Separation As a Strategy Toward Controlling Dilution Effects in Macrocyclic Glaser-Hay Couplings
    作者:Anne-Catherine Bédard、Shawn K. Collins
    DOI:10.1021/ja208902t
    日期:2011.12.14
    Macrocycles are abundant in numerous chemical applications, however the traditional strategy for the preparation of these compounds remains cumbersome and environmentally damaging; involving tedious reaction set-ups and extremely dilute reaction media. The development of a macrocyclization strategy conducted at high concentrations is described which exploits phase separation of the catalyst and substrate, as a strategy to control dilution effects. Sequestering a copper catalyst in a highly polar and/or hydrophilic phase can be achieved using a hydrophilic ligand, T-PEG(1900), a PEGylated TMEDA derivative. Similarly, phase separation is possible when suitable copper complexes are soluble in PEG(400), a green and efficient solvent which can be utilized in biphasic mixtures for promoting macrocyclization at high concentrations. The latter phase separation technique can be exploited for the synthesis of a wide range of industrially relevant macrocycles with varying ring sizes and functional groups.
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