2-(4-isobutylphenyl)-N-(3-methylphenyl)propanamide | 127460-06-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 2-(4-isobutylphenyl)-N-(3-methylphenyl)propanamide
• 英文别名: N-(3-methylphenyl)-2-[4-(2-methylpropyl)phenyl]propanamide
• CAS: 127460-06-4
• 化学式: C₂₀H₂₅NO
• 分子量: 295.4
• InChiKey: VSOVOTWMLCMLND-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-(4-异丁基苯基)丙酰氯 以92%的产率得到
  参考文献：
  名称：

  EBEID, M. Y.;AL-ASLIMAWI, M. I.;ABBAS, S. E.;ABU-KULL, M. M., EGYPT. J. PHARM. SCI., 30,(1989) N-4, C. 389-398

  摘要：

  DOI：

文献信息

• METHOD FOR PREPARING PROPANEDINITRILE OXIME ETHER COMPOUND AND INTERMEDIATE COMPOUND
  申请人：Shenyang Sinochem Agrochemicals R&D Co., Ltd.

  公开号：EP3822253A1

  公开（公告）日：2021-05-19

  Provided are a method of preparing a malononitrile oxime ether compound and an intermediate compound. The malononitrile oxime ether compound has a structure as shown in formula (VII), wherein W is selected from aryl or heteroaryl. The preparation method comprises steps: reacting a first raw material with a second raw material in the presence of a first solvent and a catalyst to obtain the intermediate compound, wherein the first raw material has a structure as shown in formula (IV), and the second raw material has a structure as shown in formula (V); and subjecting the intermediate compound as shown in formula (VI), and a dehydrant to a dehydrantion reaction in the presence of a second solvent to obtain the malononitrile oxime ether compound. In the preparation process for the intermediate, a cheaper cyanoacetamide is used as a raw material, the reaction conditions are mild. Moreover, the yield of the intermediate compound is high and the cost of the process is low. Furthermore, the required malononitrile oxime ether compound is obtained only through one-step dehydration reaction. Using the preparation method, is advantageous for improving the yield of malononitrile oxime ethers and reducing the cost of the process.

  本发明提供了一种丙二腈肟醚化合物和一种中间体化合物的制备方法。丙二腈肟醚化合物的结构如式（VII）所示，其中 W 选自芳基或杂芳基。该制备方法包括以下步骤：在第一溶剂和催化剂存在下，使第一原料与第二原料反应，得到中间体化合物，其中第一原料具有如式（IV）所示的结构，第二原料具有如式（V）所示的结构；以及在第二溶剂存在下，使如式（VI）所示的中间体化合物和脱水剂进行脱水反应，得到丙二腈肟醚化合物。在该中间体的制备过程中，使用了较为廉价的氰乙酰胺作为原料，反应条件温和。此外，中间体化合物的收率高，工艺成本低。此外，只需通过一步脱水反应就能得到所需的丙二腈肟醚化合物。该制备方法有利于提高丙二腈肟醚的产率，降低工艺成本。
• EBEID, M. Y.;AL-ASLIMAWI, M. I.;ABBAS, S. E.;ABU-KULL, M. M., EGYPT. J. PHARM. SCI., 30,(1989) N-4, C. 389-398
  作者：EBEID, M. Y.、AL-ASLIMAWI, M. I.、ABBAS, S. E.、ABU-KULL, M. M.

  DOI：——

  日期：——