2-(4-(benzyloxy)phenyl)-4H-chromen-4-one | 95161-87-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 黄酮类化合物
• 英文名称: 2-(4-(benzyloxy)phenyl)-4H-chromen-4-one
• 英文别名: 2-[4-(benzyloxy)phenyl]-4H-chromen-4-one；2-(4-benzyloxy-phenyl)-chromen-4-one；2-(4-Benzyloxy-phenyl)-chromen-4-on；4'-Benzyloxy-flavon；2-(4-Benzyloxyphenyl)chromone；2-(4-phenylmethoxyphenyl)chromen-4-one
• CAS: 95161-87-8
• 化学式: C₂₂H₁₆O₃
• 分子量: 328.367
• InChiKey: JZGKNOHKJDYNJW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(4-(benzyloxy)phenyl)-4H-chromen-4-one 在 氢溴酸 、 溶剂黄146 作用下， 生成 4-羟基黄烷酮
  参考文献：
  名称：

  213.烷酮：苯基对苄氧基苯乙烯基酮的反应活性

  摘要：

  DOI：

  10.1039/jr9390001004
• 作为产物：
  描述：

  4-苄氧基苯甲醛 在 sodium hydroxide 、 双氧水 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 96.0h， 生成 2-(4-(benzyloxy)phenyl)-4H-chromen-4-one
  参考文献：
  名称：

  Mishra; Singh, Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical, 2001, vol. 40, # 12, p. 1288 - 1294

  摘要：

  DOI：

文献信息

• One-pot synthesis of 3-haloflavones from flavones using Oxone® and potassium halide as a halogenation reagent
  作者：Tao Peng、Gang Wang、Shouguo Zhang、Yunbo Sun、Shuchen Liu、Lin Wang

  DOI：10.1016/j.tetlet.2019.151511

  日期：2020.2

  A two-step, one-pot method has been developed for the synthesis of 3-haloflavones from the corresponding flavones. The method uses Oxone® and potassium halide to produce the active molecular halogen in situ. The solvent (methanol) then participates in the reaction to afford the 2-methoxy-3-haloflavanone derivative. After adding sodium hydroxide, the corresponding 3-haloflavone product is obtained in

  已经开发了一种两步一锅法，用于从相应的黄酮合成3-卤代黄酮。该方法使用Oxone®和卤化钾原位生成活性分子卤素。然后，溶剂（甲醇）参与反应，得到2-甲氧基-3-卤代黄烷酮衍生物。加入氢氧化钠后，以良好至优异的产率获得相应的3-卤黄酮产物。该方法提供了从相同的黄酮起始原料方便地合成3-氯，3-溴和3-碘黄酮的方法。
• Silica-gel-supported Ce(SO₄)₂·4H₂O-mediated cyclization of 2′-amino and 2′-hydroxychalcones under solvent-free conditions
  作者：Ruihuan Liu、Yan Zhang、Kangping Xu、Guishan Tan

  DOI：10.1080/00397911.2016.1230217

  日期：2017.1.2

  efficient, and environmentally friendly approach for the synthesis of flavones, aza-flavones, and aza-flavanones from corresponding 2′-hydroxy or 2′-aminochalcones has been developed. The reactions are successfully conducted in presence of silica-gel-supported Ce(SO4)2·4H2O under solvent-free conditions. GRAPHICAL ABSTRACT

  摘要 我们开发了一种简单、高效且环保的方法，用于从相应的 2'-羟基或 2'-氨基查耳酮合成黄酮、氮杂黄酮和氮杂黄烷酮。该反应在硅胶负载的Ce(SO4)2·4H2O存在下，在无溶剂条件下成功进行。图形概要
• FeCl3 CATALYZED DEHYDRATIVE CYCLISATION of 1,3-(DIARYL DIKETONES) to FLAVONES
  作者：P. K. Zubaidha、A. M. Hashmi、R. S. Bhosale

  DOI：10.1515/hc.2005.11.1.97

  日期：2005.1

  required synthesis of substituted flavones on large scale. Currently there are number of methods available to synthesize flavones, among them Baker Venkatraman strategy represents the most convenient route from 2hydroxy acetophenone. In this method, acid induced dehydrative cyclisation of 1,3 ( diaryl diketones ) obtained by intramolecular Claisen condensation of Ο benzoyl acetophenone to flavones in 75%

  催化量的FeCh影响取代的1(2羟基苯基)3苯基1、3丙二醇以高产率平滑转化为相应的黄酮。简介 : 黄酮是最丰富、最重要的黄酮类化合物，具有广泛的生物活性。最近对黄酮的兴趣源于它们抑制逆转录病毒转录酶的能力以及它们抑制蛋白质酪氨酸激酶和丝氨酸/苏氨酸激酶的能力。我们对研究黄酮作为醛糖还原酶抑制剂的兴趣需要大规模合成取代的黄酮。目前有多种方法可用于合成黄酮，其中 Baker Venkatraman 策略代表了从 2-羟基苯乙酮合成最便捷的路线。在该方法中，酸诱导脱水环化 1，3（二芳基二酮）通过 Ο 苯甲酰基苯乙酮分子内克莱森缩合得到黄酮，产率为 75%。上述脱水环化的最新进展包括在 MW 辐射下使用 Amberlyst 15、Co(Sulpr) OH、Br2/CHCl3、EtOH/HCl、粘土、NaOAc/AcOH 和 H2SO4。这些程序在操作简单性、反应时间、产率和试剂成本方面受到影响
• Flavonolignan and Flavone Inhibitors of a <i>Staphylococcus </i><i>a</i><i>ureus</i> Multidrug Resistance Pump:  Structure−Activity Relationships
  作者：Nathan R. Guz、Frank R. Stermitz、Jeffrey B. Johnson、Teresa D. Beeson、Seth Willen、Jen-Fang Hsiang、Kim Lewis

  DOI：10.1021/jm0004190

  日期：2001.1.1

  Although some progress has been reported on structure-activity relationships (SARs) for inhibitors of mammalian P-glycoprotein MDR efflux pumps, there is almost nothing in the literature regarding SARs for inhibitors of any bacterial efflux pump. Indeed, only a few of these have been described. Our discovery of a potent naturally occurring flavonolignan inhibitor of the NorA MDR pump of Staphylococcus aureus provided a structural foundation upon which SARs could be assessed via synthetic analogues. Several flavonolignans were prepared which proved to have greater potency than the natural isolate, 5'-methoxyhydnocarpin-D, while others showed decreased potency. Surprisingly, some simple alkylated flavones also were quite active MDR pump inhibitors. Variability of activity among the compounds tested was sufficient so that at least some SARs could be postulated and compared with those known for P-glycoprotein.
• Synthetic Studies of Fisetin, Myricetin and Nobiletin Analogs and Related Probe Molecules
  作者：Toshiyuki Kan、Aiki Hiza、Yuta Tsukaguchi、Takahiro Ogawa、Makoto Inai、Tomohiro Asakawa、Yoshitaka Hamashima

  DOI：10.3987/com-13-s(s)107

  日期：——