[丁氧基(苯基)甲基]苯 | 7495-83-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: [丁氧基(苯基)甲基]苯
• 英文名称: n-butyl diphenylmethyl ether
• 英文别名: (butoxymethylene)dibenzene；diphenylmethyl n-butyl ether；1,1'-(Butoxymethylene)dibenzene；[butoxy(phenyl)methyl]benzene
• CAS: 7495-83-2
• 化学式: C₁₇H₂₀O
• 分子量: 240.345
• InChiKey: OPTKPWZSFJTLKB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  18
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  [丁氧基(苯基)甲基]苯 生成 1,1,2,2-四苯基乙烷
  参考文献：
  名称：

  Stadnikow, Zhurnal Russkago Fiziko-Khimicheskago Obshchestva, 1913, vol. 45, p. 1397

  摘要：

  DOI：
• 作为产物：
  描述：

  二苯基溴甲烷 在 溴甲烷 、 苯 作用下， 生成 [丁氧基(苯基)甲基]苯
  参考文献：
  名称：

  Sommelet, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1922, vol. 175, p. 1151

  摘要：

  DOI：

文献信息

• Rapid formation of diphenylmethyl ethers and thioethers using microwave irradiation and protic ionic liquids
  作者：Jarrad M. Altimari、Joshua P. Delaney、Linden Servinis、Jennifer S. Squire、Megan T. Thornton、Simren K. Khosa、Benjamin M. Long、Mark D. Johnstone、Cassandra L. Fleming、Frederick M. Pfeffer、Shane M. Hickey、Matthew P. Wride、Trent D. Ashton、Bronwyn L. Fox、Nolene Byrne、Luke C. Henderson

  DOI：10.1016/j.tetlet.2012.02.011

  日期：2012.4

  Using microwave irradiation and protic ionic liquids (pIL) as co-solvent and catalyst for the synthesis of several diphenylmethyl ethers was achieved. The desired ethers were isolated simply by filtration through a silica plug to remove the pIL and proceeded in high yields (60–98%). These reactions were extremely rapid (10–30 min) and occurred under mild conditions (80 °C). This protocol was also successfully

  使用微波辐射和质子离子液体（pIL）作为助溶剂和催化剂，合成了几种二苯甲基醚。只需通过硅胶塞过滤除去所需的pIL，即可分离出所需的醚，并以高收率（60-98％）进行。这些反应非常迅速（10–30分钟），并且在温和的条件下（80°C）发生。该方案也成功地应用于硫醚的合成。
• Aryl Boronic Acid Catalysed Dehydrative Substitution of Benzylic Alcohols for C−O Bond Formation
  作者：Susana Estopiñá‐Durán、Liam J. Donnelly、Euan B. Mclean、Bryony M. Hockin、Alexandra M. Z. Slawin、James E. Taylor

  DOI：10.1002/chem.201806057

  日期：2019.3.12

  substitution of benzylic alcohols with a second alcohol to form new C−O bonds. This method has been applied to the intermolecular substitution of benzylic alcohols to form symmetrical ethers, intramolecular cyclisations of diols to form aryl‐substituted tetrahydrofuran and tetrahydropyran derivatives, and intermolecular crossed‐etherification reactions between two different alcohols. Mechanistic control

  五氟苯基硼酸和草酸的组合催化苄醇与第二种醇的脱水取代，形成新的C-O键。该方法已应用于苯甲醇的分子间取代以形成对称醚，二醇的分子内环化以形成芳基取代的四氢呋喃和四氢吡喃衍生物，以及两种不同醇之间的分子间交叉醚化反应。机械控制实验已经确定了在芳基硼酸和草酸之间形成的潜在催化中间体。
• Direct and efficient synthesis of unsymmetrical ethers from alcohols catalyzed by Fe(HSO4)3 under solvent‐free conditions
  作者：Bashir Nazari Moghadam、Batool Akhlaghinia、Soodabeh Rezazadeh

  DOI：10.1007/s11164-015-2098-y

  日期：2016.2

  Highly efficient Fe(HSO4)3 catalyzed etherification of primary, secondary and tertiary benzylic alcohols with primary and secondary aliphatic alcohols is reported. The reaction affords unsymmetrical benzyl ethers in good to excellent yields under solvent-free conditions.

  报道了伯，仲和叔苄醇与伯和仲脂族醇的高效Fe（HSO 4）3催化醚化。该反应在无溶剂条件下以良好或优异的产率提供不对称的苄基醚。
• Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including <i>p</i>-methoxybenzyl ethers of alcohols and phenols
  作者：Kamlesh V. Katkar、Sachin D. Veer、Krishnacharya G. Akamanchi

  DOI：10.1080/00397911.2016.1230218

  日期：2016.12.1

  ABSTRACT Sulfated tungstate was found to be an effective heterogeneous and reusable catalyst for hydroxy group activation–mediated preparation of benzylic ethers including p-methoxybenzylic ethers of a wide range of alcohols and phenols under mild reaction conditions. GRAPHICAL ABSTRACT

  摘要 硫酸化钨酸盐被发现是一种有效的多相和可重复使用的催化剂，用于在温和的反应条件下羟基活化介导的苄醚制备，包括各种醇和酚的对甲氧基苄醚。图形概要
• Chemoselective Formation of Unsymmetrically Substituted Ethers from Catalytic Reductive Coupling of Aldehydes and Ketones with Alcohols in Aqueous Solution
  作者：Nishantha Kalutharage、Chae S. Yi

  DOI：10.1021/acs.orglett.5b00553

  日期：2015.4.3

  A well-defined cationic Ru–H complex catalyzes reductive etherification of aldehydes and ketones with alcohols. The catalytic method employs environmentally benign water as the solvent and cheaply available molecular hydrogen as the reducing agent to afford unsymmetrical ethers in a highly chemoselective manner.

  定义明确的阳离子Ru–H络合物催化醛和酮与醇的还原醚化反应。该催化方法使用环境友好的水作为溶剂，使用廉价的分子氢作为还原剂，以高度化学选择性的方式提供不对称醚。