α-(4-nitrophenoxy)acetophenone | 18065-03-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: α-(4-nitrophenoxy)acetophenone
• 英文别名: 2-(4-nitrophenoxy)-1-phenyl-ethanone；ω-(p-Nitro-phenoxy)-acetophenon；2-(4-Nitrophenoxy)-1-phenylethanone
• CAS: 18065-03-7
• 化学式: C₁₄H₁₁NO₄
• mdl: MFCD00430565
• 分子量: 257.246
• InChiKey: QKYYIECVXQTDPV-UHFFFAOYSA-N

物化性质

• 熔点：
  148-149 °C
• 沸点：
  445.5±25.0 °C(Predicted)
• 密度：
  1.278±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  19
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  α-(4-nitrophenoxy)acetophenone 在 溴 作用下， 以 溶剂黄146 为溶剂， 生成 ω-(4-Nitro-phenoxy)-ω-acetoxy-acetophenon
  参考文献：
  名称：

  Kroehnke,F. et al., Journal fur praktische Chemie (Leipzig 1954), 1960, vol. 11, p. 249 - 255

  摘要：

  DOI：
• 作为产物：
  描述：

  苯乙酮 在 溴 、 potassium carbonate 作用下， 以 氯仿 、 丁酮 为溶剂， 反应 2.25h， 生成 α-(4-nitrophenoxy)acetophenone
  参考文献：
  名称：

  Synthesis, Characterization and in vitro Anticancer Activity of Novel 8,4’-Oxyneolignan Analogues

  摘要：

  Neolignans are a class of natural products with a wide range of biological effects. These substances are of great synthetic and biological interest, especially in searching for novel anticancer agents. In this paper, we report the synthesis of a new subclass of 8,4'-oxyneolignan analogues (beta-ketoethers and beta-ketoesters) and their cell viability assay on twenty four different cancer cells, among leukemias and carcinomas. Three compounds inhibited the growth of most human cancer cells. 2-Oxo-2-phenylethyl(2E)-3-[4-(2-oxo-2-phenylethoxy) phenyl] prop-2-enoate showed an antiproliferative activity superior to doxorubicin for U-87, U-138 MG and H1299 cell types and (E)-2-oxo-2-phenylethyl 3-(3-methoxy-4-(2-oxo-2-phenylethoxy) phenyl) acrylate was found to be very selective, demonstrating a growth inhibition of 92.0% against KG-1 cells. Furthermore, 1-oxo-1-phenylpropan-2-yl cinnamate exhibited significant inhibition activity in a range of 52.2 to 91.2% against twelve kinds of leukemia cell lines, revealing excellent results and very comparable to the reference drug.

  DOI：

  10.21577/0103-5053.20170075

文献信息

• Three-step synthesis of an array of substituted benzofurans using polymer-supported reagents
  作者：Jörg Habermann、Steven V. Ley、René Smits

  DOI：10.1039/a904384e

  日期：——

  achieved by the bromination of acetophenones to α-bromoacetophenones by polymer-supported pyridinium bromide perbromide (PSPBP). The subsequent clean substitution of the obtained bromides by phenols using 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD-P) and cyclodehydration of the resulting α-phenoxyacetophenones using Amberlyst 15, affords pure products without the need for any chromatographic purification

  通过用聚合物负载的溴化吡啶鎓过溴化物（PSPBP）将苯乙酮溴化为α-溴苯乙酮，可以实现一种有效的组合方法，以取代3-苯基苯并呋喃。随后使用1,5,7-三氮杂双环[4.4.0]癸-5-烯（TBD-P）将所得的溴化物彻底替换为苯酚，并使用Amberlyst 15将所得的α-苯氧基乙酰苯酮环化脱水，得到的纯产品不含需要任何色谱纯化步骤。
• I2-mediated and direct synthesis of 3-phenoxy imidazo heterocycles
  作者：Yanchun Guo、Yuexiu Wang、Han Xue、Shuxia Cao、Yufen Zhao

  DOI：10.1016/j.tet.2019.01.066

  日期：2019.3

  An I2-mediated protocol was proposed for the synthesis of 3-phenoxy imidazo heterocycles from aromatic ketones and 2-aminopyridines or 2-aminobenzothiazole. This direct, efficient and operationally simple method provided a fundamentally novel and rapid approach for the synthesis of 3-phenoxy imidazo heterocycles with good to excellent yields, and it avoided the requirement of any metal, base and extra

  提出了一种I 2介导的方案，用于从芳族酮和2-氨基吡啶或2-氨基苯并噻唑合成3-苯氧基咪唑杂环。这种直接，有效和操作简单的方法为合成3-苯氧基咪唑并具有极佳的产率提供了根本上新颖且快速的方法，并且避免了对任何金属，碱和额外氧化剂的需求。
• Synthesis of benzofurans from the cyclodehydration of α-phenoxy ketones mediated by Eaton’s reagent
  作者：Zhanwei Ma、Min Zhou、Lin Ma、Min Zhang

  DOI：10.1177/1747519820907244

  日期：2020.7

  acid) is used to prepare 3-substituted or 2,3-disubstituted benzofurans with moderate to excellent yields under mild conditions. The method provides a facile access to benzofurans from readily available starting materials such as phenols and α-bromo ketones. The reaction is highly efficient, which is attributed to the good reactivity and fluidity of Eaton’s reagent. The reaction can be applied to prepare

  由伊顿试剂（五氧化二磷-甲磺酸）促进的 α-苯氧基酮的环脱水用于在温和条件下以中等至优异的产率制备 3-取代或 2,3-二取代的苯并呋喃。该方法提供了从容易获得的起始材料（如苯酚和 α-溴酮）中轻松获得苯并呋喃的途径。反应效率高，这归功于伊顿试剂良好的反应性和流动性。该反应可用于制备萘并呋喃香豆素、苯并噻吩和苯并吡喃。
• New Heterocyclic Precursors for Thermal Generation of Reactive, Electron-Rich 1,2-Diaza-1,3-butadienes
  作者：Robert K. Boeckman,、Ping Ge、Jessica E. Reed

  DOI：10.1021/ol0165645

  日期：2001.11.1

  [reaction--see text] [corrected] The preparation and thermolysis of new stable heterocyclic precursors of 1,2-diaza-1,3-butadienes is described. The resulting reactive diazadienes are trapped in situ with N-phenylmaleimide [corrected]. The effect of precursor structure on the temperature at which the diazadienes are generated is discussed.

  [反应-见正文] [已更正]描述了1,2-二氮杂-1,3-丁二烯新的稳定杂环前体的制备和热解。生成的反应性二氮杂二烯被N-苯基马来酰亚胺原位捕获[校正]。讨论了前体结构对生成二氮杂二烯的温度的影响。
• Synthesis, characterization, and third-order nonlinear optical properties of a new neolignane analogue
  作者：Wesley F. Vaz、Jean M. F. Custodio、Rafael G. Silveira、Adailton N. Castro、Carlos E. M. Campos、Murilo M. Anjos、Guilherme R. Oliveira、Clodoaldo Valverde、Basílio Baseia、Hamilton B. Napolitano

  DOI：10.1039/c6ra14961h

  日期：——

  This paper presents an extensive study of a new neolignane analogue using experimental and theoretical approach and brings highlights in solid state characterization and electronic properties.

  本文使用实验和理论方法对新型新木质素类似物进行了广泛的研究，并在固态表征和电子性能方面提出了亮点。