3-hydroxy-3-(4-nitro-phenyl)-propionic acid methyl ester | 135505-17-8

• 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: 3-hydroxy-3-(4-nitro-phenyl)-propionic acid methyl ester
• 英文别名: 3-Hydroxy-3-(4-nitro-phenyl)-propionsaeure-methylester；Methyl 3-hydroxy-3-(4-nitrophenyl)propanoate
• CAS: 135505-17-8
• 化学式: C₁₀H₁₁NO₅
• 分子量: 225.201
• InChiKey: OBFIKZLNFXSNNQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  92.4
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  甲醇 、 3-hydroxy-3-(4-nitrophenyl)propanoic acid 在 zinc(II) chloride 作用下， 生成 3-hydroxy-3-(4-nitro-phenyl)-propionic acid methyl ester
  参考文献：
  名称：

  Einhorn; Prausnitz, Chemische Berichte, 1884, vol. 17, p. 1660,1661

  摘要：

  DOI：

文献信息

• Method for synthesizing chiral beta-hydroxy acid ester compound
  申请人：Wenzhou University

  公开号：US10906860B2

  公开（公告）日：2021-02-02

  A method for synthesizing a chiral β-hydroxy acid ester compound is disclosed. The method includes the steps of: using an aldehyde compound and a monoalkyl malonate as raw materials, using a metal and a chiral ligand as a catalyst to make the raw materials be directly and fully reacted in an organic solvent and form a reaction solution, and separating and purifying the reaction solution to obtain the highly stereoselective β-hydroxy acid ester compound. The beneficial effects are mainly embodied in: 1. simple operation; 2. rapidly constructing a highly stereoselective β-hydroxy acid ester skeleton structure molecule; 3. high reaction yield and good stereoselectivity. Therefore, the invention has high basic research significance, industrial production value and social economic benefit.

  本发明公开了一种合成手性β-羟基酸酯化合物的方法。该方法包括以下步骤：以醛类化合物和丙二酸单烷基酯为原料，以金属和手性配体为催化剂，使原料在有机溶剂中直接充分反应，形成反应溶液，分离纯化反应溶液，得到高立体选择性的β-羟基酸酯化合物。其优点主要体现在1.操作简单；2.快速构建高立体选择性的β-羟基酸酯骨架结构分子；3.反应产率高，立体选择性好。因此，本发明具有较高的基础研究意义、工业生产价值和社会经济效益。
• METHOD FOR SYNTHESIZING CHIRAL BETA-HYDROXY ACID ESTER COMPOUND
  申请人：Wenzhou University

  公开号：US20200190013A1

  公开（公告）日：2020-06-18

  A method for synthesizing a chiral β-hydroxy acid ester compound is disclosed. The method includes the steps of: using an aldehyde compound and a monoalkyl malonate as raw materials, using a metal and a chiral ligand as a catalyst to make the raw materials be directly and fully reacted in an organic solvent and form a reaction solution, and separating and purifying the reaction solution to obtain the highly stereoselective β-hydroxy acid ester compound. The beneficial effects are mainly embodied in: 1. simple operation; 2. rapidly constructing a highly stereoselective β-hydroxy acid ester skeleton structure molecule; 3. high reaction yield and good stereoselectivity. Therefore, the invention has high basic research significance, industrial production value and social economic benefit.
• Einhorn; Prausnitz, Chemische Berichte, 1884, vol. 17, p. 1660,1661
  作者：Einhorn、Prausnitz

  DOI：——

  日期：——