4-hydroxy-N-(4-methylphenyl)-butanamide

• 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: 4-hydroxy-N-(4-methylphenyl)-butanamide
• 英文别名: 4-hydroxy-N-(4-methylphenyl)butanamide
• 化学式: C₁₁H₁₅NO₂
• 分子量: 193.246
• InChiKey: PXYLPVZFIIKRHI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  49.3
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-hydroxy-N-(4-methylphenyl)-butanamide 生成 1-(4-甲基苯基)-2-吡咯烷酮
  参考文献：
  名称：

  KURBANOV P.; KADYROV CH. SH., UZSSR FANLAR AKAD. DOKL., DOKL. AN UZSSR, 1981, HO 6, 39-40

  摘要：

  DOI：
• 作为产物：
  描述：

  N-(4-methylphenyl)succinamide methyl ester 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 生成 4-hydroxy-N-(4-methylphenyl)-butanamide
  参考文献：
  名称：

  Kumar, Padam Praveen; Reddy, Y. Dathu; Kumari, Y. Bharathi, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2014, vol. 53, # 4, p. 392 - 398

  摘要：

  DOI：

文献信息

• Metal‐Free Synthesis of <i>N</i> ‐Aryl Amides using Organocatalytic Ring‐Opening Aminolysis of Lactones
  作者：Wusheng Guo、José Enrique Gómez、Luis Martínez‐Rodríguez、Nuno A. G. Bandeira、Carles Bo、Arjan W. Kleij

  DOI：10.1002/cssc.201700415

  日期：2017.5.9

  Catalytic ring‐opening of bio‐sourced non‐strained lactones with aromatic amines can offer a straightforward, 100 % atom‐economical, and sustainable pathway towards relevant N‐aryl amide scaffolds. Herein, the first general, metal‐free, and highly efficient N‐aryl amide formation is reported from poorly reactive aromatic amines and non‐strained lactones under mild operating conditions using an organic

  生物来源的非应变内酯与芳族胺的催化开环可以提供一种直接的，100％原子经济且可持续的通往相关N芳基酰胺支架的途径。在此，据报道，在温和的操作条件下，使用有机双环胍催化剂，由反应性较差的芳族胺和非应变的内酯首次形成了无金属且高效的N-芳基酰胺。该协议具有很高的应用潜力，例如与药物相关的分子的形式合成。
• Ruthenium-catalyzed synthesis of <i>N</i>-substituted lactams by acceptorless dehydrogenative coupling of diols with primary amines
  作者：Yanling Zheng、Xufeng Nie、Yang Long、Li Ji、Haiyan Fu、Xueli Zheng、Hua Chen、Ruixiang Li

  DOI：10.1039/c9cc06339k

  日期：——

  Herein, we report the first example of synthesis of N-substituted lactams via an acceptorless dehydrogenative coupling of diols with primary amines in one step, which was enabled by combining Ru3(CO)12 with a hybrid N-heterocyclic carbene–phosphine–phosphine ligand as the catalyst.

  在本文中，我们报道的合成的第一示例Ñ取代的内酰胺通过与伯胺二醇的acceptorless脱氢偶联在一个步骤中，将其通过钌组合启用3（CO）12与混合动力N-杂环卡宾-膦膦配体作为催化剂。
• Organotin-catalyzed synthesis of hydroxyalkylamides from lactones via a ring-opening process
  作者：Xiayu Liang、Peng Yu、Chen Fu、Yongcun Shen

  DOI：10.1016/j.tetlet.2021.152821

  日期：2021.3

  A new strategy for the facile synthesis of hydroxyalkylamides through the ring-opening reaction of lactone with amine promoted by dibutyltin acetate was developed. A series of hydroxyalkylamide compounds were obtained and the method was successfully applied to the synthesis of pharmaceutically active molecules tyrosinase inhibitor V and HDAC inhibitor VI via a three-step synthetic pathway. The broad

  提出了通过乙酸二丁锡促进内酯与胺的开环反应轻松合成羟烷基酰胺的新策略。获得了一系列羟烷基酰胺化合物，并将该方法成功地通过三步合成途径用于合成药物活性分子酪氨酸酶抑制剂V和HDAC抑制剂VI。广泛的底物范围，温和的反应条件和实际应用证明了该方法的有效性，兼容性和实用性。
• One‐Pot Syntheses of Amides from N‐Acylation of Nitroarenes with Esters Mediated by Samarium Diiodide
  作者：Xiaoxia Wang、Hongyun Guo、Guanqun Xie、Yongmin Zhang

  DOI：10.1081/scc-200026659

  日期：2004.1.1

  Abstract Mediated by samarium diiodide, various amides were prepared directly from nitroarenes and esters under mild conditions in a one‐pot procedure.

  摘要 在二碘化钐的介导下，以硝基芳烃和酯类为原料，在温和条件下，通过一锅法直接制备了各种酰胺。
• Kumar, Padam Praveen; Reddy, Y. Dathu; Kumari, Y. Bharathi, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2014, vol. 53, # 4, p. 392 - 398
  作者：Kumar, Padam Praveen、Reddy, Y. Dathu、Kumari, Y. Bharathi、Devi, B. Rama、Dubey

  DOI：——

  日期：——