3-(naphthalen-1-yl)-2H-chromen-2-one | 42189-35-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 3-(naphthalen-1-yl)-2H-chromen-2-one
• 英文别名: 3-Naphthalen-1-ylchromen-2-one
• CAS: 42189-35-5
• 化学式: C₁₉H₁₂O₂
• 分子量: 272.303
• InChiKey: XRWFDOUOZHEORC-UHFFFAOYSA-N

物化性质

• 熔点：
  154-155 °C(Solv: methanol (67-56-1))
• 沸点：
  495.6±24.0 °C(Predicted)
• 密度：
  1.276±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  1-萘乙酸 在 1-n-butyl-3-methylimidazolium tetrafluoroborate 作用下， 反应 2.5h， 生成 3-(naphthalen-1-yl)-2H-chromen-2-one
  参考文献：
  名称：

  Facile one-pot synthetic access to libraries of diversely substituted 3-aryl (Alkyl)-coumarins using ionic liquid (IL) or conventional base/solvent, and an IL-mediated approach to novel coumarin-bearing diaryl-ethynes

  摘要：

  The in-situ formed carbonylimidazole derivatives of Ar(alkyl)-CH2COOH react at r.t. with substituted salicylaldehydes in [BMIM][PF6] or [BMIM] [BEd as solvent, and [PAIM][NTf (2)] as basic-IL to produce libraries of 3-aryl(alkyl)coumarins. Whereas these reactions can also be performed with similar efficiency in THF by employing DBU, the IL approach offers easier work-up and recycling of the IL solvent. An IL-mediated approach to the synthesis of novel coumarin-bearing diaryl-ethynes by the Sonogshira reaction is also reported, and the potential for recycling/reuse of the IL solvent is shown. (C) 2020 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2020.151854

文献信息

• Pd-catalysed carbonylative annulation of salicylaldehydes with benzyl chlorides using<i>N</i>-formylsaccharin as a CO surrogate
  作者：Vinod K. Yadav、Vishnu P. Srivastava、Lal Dhar S. Yadav

  DOI：10.1039/c8nj03173h

  日期：——

  A highly efficient synthesis of 3-arylcoumarins by Pd-catalysed carbonylative cyclisation of salicylaldehydes with benzyl chlorides usingN-formylsaccharin as a CO source is developed.

  以 N-甲酰基糖精为 CO 源，通过 Pd 催化水杨醛与苄基氯的羰基化环化，开发了一种高效合成 3-芳基香豆素的方法。
• KMnO₄/AcOH-mediated C3-selective direct arylation of coumarins with arylboronic acids
  作者：Jin-Wei Yuan、Liang-Ru Yang、Qiu-Yue Yin、Pu Mao、Ling-Bo Qu

  DOI：10.1039/c6ra04787d

  日期：——

  dehydrogenative direct radical arylation of coumarins with arylboronic acids to afford 3-arylcoumarin derivatives is described. A similar reaction system is also applicable to the 3-arylation of quinolinone derivatives. These KMnO4/AcOH-mediated coupling reactions occur regioselectively at the C3 position of coumarins and quinolinones. Some notable features of this method are high efficiency, moderate

  描述了一种有效的方案，用于香豆素与芳基硼酸的KMnO 4 / AcOH介导的脱氢直接自由基芳基化，以提供3-芳基香豆素衍生物。类似的反应系统也适用于喹啉酮衍生物的3-芳基化。这些KMnO 4 / AcOH介导的偶联反应在香豆素和喹啉酮的C3位置区域选择性地发生。该方法的一些显着特征是效率高，产量中等到良好以及广泛的群体耐受性。
• Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes
  作者：Yuansong Jiang、Wanzhi Chen、Weimin Lu

  DOI：10.1016/j.tet.2013.03.025

  日期：2013.5

  The condensation reaction of 2-chloro-2-arylacetaldehyde with salicylaldehyde catalyzed by N-heterocyclic carbene (NHC) leading to 3-arylcoumarin was studied. A number of 3-arylcoumarin derivatives were obtained in good to excellent yields via this umpolung reaction. This reaction is facile and experimentally simple and mild.

  研究了N-杂环卡宾（NHC）催化2-氯-2-芳基乙醛与水杨醛的缩合反应，生成3-芳基香豆素。通过这种化学反应，以良好的产率获得了许多3-芳基香豆素衍生物。该反应是容易的，并且实验上简单温和。
• A General Palladium-Catalyzed Carbonylative Synthesis of Chromenones from Salicylic Aldehydes and Benzyl Chlorides
  作者：Xiao-Feng Wu、Lipeng Wu、Ralf Jackstell、Helfried Neumann、Matthias Beller

  DOI：10.1002/chem.201301774

  日期：2013.9.9

  Cute CO! An interesting and straightforward procedure for the carbonylative synthesis of chromenones from readily available salicylic aldehydes and benzyl chlorides has been developed (see scheme; DPPP=1,3‐bis(diphenylphosphino)propane). In the presence of a palladium catalyst, various coumarins were produced in good to excellent yields.

  可爱的CO！已经开发了一种有趣且简单的方法，可以从容易获得的水杨醛和苄基氯羰基合成羰基壬烯（见方案； DPPP = 1,3-双（二苯基膦基）丙烷）。在钯催化剂的存在下，以良好至优异的产率制备了各种香豆素。
• Three-component coupling using arynes and DMF: straightforward access to coumarins via ortho-quinone methides
  作者：Hiroto Yoshida、Yu Ito、Joji Ohshita

  DOI：10.1039/c1cc11955a

  日期：——

  ortho-Quinone methides, arising from a formal [2+2] cycloaddition between arynes and DMF, were found to facilely undergo a [4+2] cycloaddition with ester enolates or ketenimine anions to produce diverse coumarins in a straightforward manner.

  ortho-奎宁美酸甲酯是通过芳香烃与DMF之间的形式[2+2]环加成反应生成的，发现它们能够轻松地与酯烯醇盐或酮亚胺阴离子进行[4+2]环加成反应，从而以简单的方式生成多样化的香豆素。