1-p-Tolyl-cycloheptanol | 77826-31-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-p-Tolyl-cycloheptanol
• 英文别名: 1-(4-Methylphenyl)cycloheptan-1-ol
• CAS: 77826-31-4
• 化学式: C₁₄H₂₀O
• 分子量: 204.312
• InChiKey: OFZRFGIPUPNDMN-UHFFFAOYSA-N

物化性质

• 沸点：
  331.8±11.0 °C(Predicted)
• 密度：
  1.021±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-p-Tolyl-cycloheptanol 在 对甲苯磺酸 、 臭氧 作用下， 以 甲苯 为溶剂， 生成 7-(4-甲基苯基)-7-氧代庚酸
  参考文献：
  名称：

  Hydrophobic-hydrophilic interactions in sodium dodecyl sulfate micelles. Stilbene-viologen complex formation as a probe of the micelle interior

  摘要：

  DOI：

  10.1021/ja00401a053
• 作为产物：
  描述：

  对溴甲苯 、 环庚酮 在 碘 、 magnesium 作用下， 以 乙醚 为溶剂， 反应 2.0h， 生成 1-p-Tolyl-cycloheptanol
  参考文献：
  名称：

  Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes

  摘要：

  Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes to a new series of [7-6-6] tricyclic system were described. A variety of substituents at the para-position of the phenyl were amenable to this transformation, including electron-donating groups and halides. The presence of electron-donating groups resulted in a more efficient reaction, with higher yields than the case of halides. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.03.023

文献信息

• Iodobenzene-catalyzed oxidative cleavage of olefins to carbonyl compounds
  作者：Lele Du、Zechao Wang、Junliang Wu

  DOI：10.1016/j.tetlet.2020.152204

  日期：2020.8

  A metal-free approach for the oxidative cleavage of carbon–carbon double bonds of olefins to carbonyl compounds was established by using oxidant m-CPBA and non-metallic organocatalyst PhI in toluene/H2O. A broad scope of aromatic olefins was used. All the reactions proceeded smoothly at 35 °C in short reaction time to furnish the respective mono- and double carbonyl compounds selectively in moderate

  通过使用氧化剂m -CPBA和甲苯/ H 2 O中的非金属有机催化剂PhI，建立了一种无金属的方法将烯烃的碳-碳双键氧化裂解为羰基化合物。使用了广泛的芳族烯烃。所有反应均在35°C的短时间内顺利进行，以中等至良好的收率选择性提供各自的单羰基化合物和双羰基化合物。
• Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes
  作者：Gon-Ann Lee、Hsin-Yi Lee、Wen-Chieh Wang、Chih-Hwa Cherng

  DOI：10.1016/j.tet.2014.03.023

  日期：2014.5

  Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes to a new series of [7-6-6] tricyclic system were described. A variety of substituents at the para-position of the phenyl were amenable to this transformation, including electron-donating groups and halides. The presence of electron-donating groups resulted in a more efficient reaction, with higher yields than the case of halides. (C) 2014 Elsevier Ltd. All rights reserved.
• Hydrophobic-hydrophilic interactions in sodium dodecyl sulfate micelles. Stilbene-viologen complex formation as a probe of the micelle interior
  作者：John C. Russell、David G. Whitten、Andre M. Braun

  DOI：10.1021/ja00401a053

  日期：1981.6