[4-[[2-[[4-(Hydroxymethyl)phenoxy]methyl]phenyl]methoxy]phenyl]methanol | 170651-95-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: [4-[[2-[[4-(Hydroxymethyl)phenoxy]methyl]phenyl]methoxy]phenyl]methanol
• CAS: 170651-95-3
• 化学式: C₂₂H₂₂O₄
• 分子量: 350.414
• InChiKey: XBMYBVUKAUGVIL-UHFFFAOYSA-N

物化性质

• 沸点：
  565.1±45.0 °C(Predicted)
• 密度：
  1.223±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  26
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  58.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  [4-[[2-[[4-(Hydroxymethyl)phenoxy]methyl]phenyl]methoxy]phenyl]methanol 在 三溴化磷 、 硫脲 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 36.0h， 生成 [4-[[2-[[4-(Sulfanylmethyl)phenoxy]methyl]phenyl]methoxy]phenyl]methanethiol
  参考文献：
  名称：

  环内连接双环环烷的合成与络合研究

  摘要：

  用二硫代硫酸钠还原衍生自2,6-双（氯甲基）苯醌和合适的二硫醇的环烷，然后进一步与各种二溴化物偶合，得到环内连接的双环环烷，与TCNQ和TCNE形成电荷转移配合物。

  DOI：

  10.1016/j.tet.2006.07.064
• 作为产物：
  描述：

  1,2-benzyloxy-bis-(4-benzaldehyde) 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 反应 6.0h， 以90%的产率得到[4-[[2-[[4-(Hydroxymethyl)phenoxy]methyl]phenyl]methoxy]phenyl]methanol
  参考文献：
  名称：

  Dioxastilbenophanes—synthesis and charge transfer complexation studies

  摘要：

  Intramolecular McMurry coupling of dialdehydes derived from xylenyl dibromide and 4-hydroxy benzaldehyde afforded cis-stilbenophanes along with cyclophane diols. Stilbenophanes with a large cavity were also synthesized. Charge transfer complexations of the stilbenophanes with TCNE, TCNQ and PQT were studied. Some stilbenophanes form a relatively stronger complex with PQT rather than with TCNE and TCNQ. (C) 2004 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2004.01.008

文献信息

• Synthesis of Cyclophanes with Intra-Annular Functionality and Cage Structure
  作者：Arunachalam Kannan、Perumal Rajakumar、V. Kabaleeswaran、S. S. Rajan

  DOI：10.1021/jo950957y

  日期：1996.1.1

  Cyclophanes of the type 1 and 2, with large cavity sizes, have been synthesized from the corresponding dichloride 8 or 8a and o-xylene-alpha,alpha'-dithiol (9), p-xylene-alpha,alpha'-dithiol (10), or m-terphenyldithiol (11). Similarly, cyclophanes of the type 3 with intra-annular functionality have been obtained by the coupling of the corresponding dithiol 15 or 19 and m-terphenyl dibromide 5, 5a, 5b, or 5c. With the aim of introducing multifunctionality, cyclophanes of the type 21 and 23 were prepared from 3,5-bis(mercaptomethyl)anisole or 3,5-bis(mercaptomethyl)phenol and the corresponding substituted m-terphenyl dibromide Bb or 5c. Cyclophanes 24, 24a, 24b, and 32, with a new type of cage structure, have been obtained by the coupling of the corresponding tetrathiol as with 2 equiv of the dibromides 5c, 5a, and 5b or 1 equiv of the tetrabromide 31, respectively. Further, the sodium salts of the cyclophanes 3c, 21, and 24b were completely characterized by H-1 NMR spectroscopy. XRD analysis of the cyclophane 21 revealed the presence of an ethanol molecule inside the cavity, indicating the facile formation of a host-guest complex.
• Synthesis and Molecular Transformations of Functionalised Cyclophanes with Large Cavity
  作者：Arunachalam Kannan、Perumal Rajakumar

  DOI：10.1080/00397919508011438

  日期：1995.10

  Cyclophanes of the type 1 & 3 are obtained by the coupling of suitable dithiol with corresponding dibromide under high dilution technique in the presence of KOH in benzene or toluene-ethanol. Few molecular transformations have been effected on the cyclophanes 1 and 2.