2-Propoxycarbonylfuran-3-carboxylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 呋喃
• 英文名称: 2-Propoxycarbonylfuran-3-carboxylic acid
• 英文别名: 2-propoxycarbonylfuran-3-carboxylic acid
• 化学式: C₉H₁₀O₅
• 分子量: 198.17
• InChiKey: OOXPHDJPHYPNNE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  14
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  76.7
• 氢给体数：
  1
• 氢受体数：
  5

文献信息

• Esterification of 2,5-furan-dicarboxylic acid
  申请人：Archer Daniels Midland Company

  公开号：US10155736B2

  公开（公告）日：2018-12-18

  A method of making a furan dicarboxylate by means of reacting 2,5-furan dicarboxylic acid (FDCA) with an alcohol or mixture of alcohols in a CO2-predominant atmosphere without the presence of any other acid catalyst is described. The reaction is conducted under conditions that correspond to either supercritical, critical or near-critical temperatures and pressures for the alcohol species and/or CO2 gas.

  本发明描述了一种在不使用任何其他酸催化剂的情况下，在以二氧化碳为主的气氛中通过 2,5-呋喃二羧酸（FDCA）与醇或醇混合物反应来制造呋喃二甲酸酯的方法。反应是在醇类和/或二氧化碳气体的超临界、临界或近临界温度和压力条件下进行的。
• ESTERIFICATION OF 2,5-FURAN-DICARBOXYLIC ACID
  申请人：Archer Daniels Midland Company

  公开号：EP2935229A2

  公开（公告）日：2015-10-28
• Esterification of 2,5-Furan-Dicarboxylic Acid
  申请人：ARCHER DANIELS MIDLAND COMPANY

  公开号：US20150315166A1

  公开（公告）日：2015-11-05

  A method of making a furan dicarboxylate by means of reacting 2,5-furan dicarboxylic acid (FDCA) with an alcohol or mixture of alcohols in a CO 2 -predominant atmosphere without the presence of any other acid catalyst is described. The reaction is conducted under conditions that correspond to either supercritical, critical or near-critical temperatures and pressures for the alcohol species and/or CO 2 gas.
• US9765045B2
  申请人：——

  公开号：US9765045B2

  公开（公告）日：2017-09-19
• [EN] ESTERIFICATION OF 2,5-FURAN-DICARBOXYLIC ACID<br/>[FR] ESTÉRIFICATION D'ACIDE 2,5-FURAN-DICARBOXYLIQUE
  申请人：ARCHER DANIELS MIDLAND CO

  公开号：WO2014099438A2

  公开（公告）日：2014-06-26

  A method of making a furan dicarboxylate by means of reacting 2,5-furan dicarboxylic acid (FDCA) with an alcohol or mixture of alcohols in a CO2-predominant atmosphere without the presence of any other acid catalyst is described. The reaction is conducted under conditions that correspond to either supercritical, critical or near-critical temperatures and pressures for the alcohol species and/or CO2 gas.