N,N-dibenzyloctanamide

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: N,N-dibenzyloctanamide
• 化学式: C₂₂H₂₉NO
• 分子量: 323.478
• InChiKey: FKPPBRVRCMKMTC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  24
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  辛酸 、 二苄胺 在 1,8-双二甲氨基萘 、 ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 以67%的产率得到N,N-dibenzyloctanamide
  参考文献：
  名称：

  XtalFluor-E, an Efficient Coupling Reagent for Amidation of Carboxylic Acids

  摘要：

  Amides were produced from carboxylic acids and amines by using XtalFluor-E as an activator. Even poorly reactive carboxylic acids can be transformed to amides. In addition, optically active amines and/or carboxylic acids were not epimerized/racemized during the process.

  DOI：

  10.1021/ol400045d

文献信息

• PROCESS FOR THE PREPARATION OF GLYCOLALDEHYDE
  申请人：Puckette Thomas Allen

  公开号：US20080081759A1

  公开（公告）日：2008-04-03

  Disclosed are catalyst solutions for the hydroformylation of formaldehyde comprising one or more fluorophosphite compounds, rhodium and a hydroformylation solvent comprising at least one N,N-disubstituted amide, N-substituted cyclic amide, or a mixture thereof. Also disclosed are hydroformylation processes wherein formaldehyde is contacted with carbon monoxide, hydrogen one or more fluorophosphite compounds, rhodium and a hydroformylation solvent to produce glycolaldehyde. The fluorophosphite-based catalysts provide good reaction rates and high selectivity to glycolaldehyde.
• US4115204A
  申请人：——

  公开号：US4115204A

  公开（公告）日：1978-09-19
• US7301054B1
  申请人：——

  公开号：US7301054B1

  公开（公告）日：2007-11-27
• XtalFluor-E, an Efficient Coupling Reagent for Amidation of Carboxylic Acids
  作者：Aurélie Orliac、Domingo Gomez Pardo、Agnès Bombrun、Janine Cossy

  DOI：10.1021/ol400045d

  日期：2013.2.15

  Amides were produced from carboxylic acids and amines by using XtalFluor-E as an activator. Even poorly reactive carboxylic acids can be transformed to amides. In addition, optically active amines and/or carboxylic acids were not epimerized/racemized during the process.