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N-decyl-15-hydroxypentadecanoylamine | 1220909-18-1

中文名称
——
中文别名
——
英文名称
N-decyl-15-hydroxypentadecanoylamine
英文别名
——
N-decyl-15-hydroxypentadecanoylamine化学式
CAS
1220909-18-1
化学式
C25H51NO2
mdl
——
分子量
397.685
InChiKey
OPGZNDRVPCTDAC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.31
  • 重原子数:
    28.0
  • 可旋转键数:
    23.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    49.33
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    环十五内酯1-氨基癸烷 在 lipase PS from Pseudomonas cepacia 、 作用下, 以 正十六烷 为溶剂, 反应 192.0h, 以88%的产率得到N-decyl-15-hydroxypentadecanoylamine
    参考文献:
    名称:
    Enzymatic aminolysis of lactones in aqueous miniemulsion: Catalysis through a novel pathway
    摘要:
    Lipase-catalyzed aminolysis of lactones under aqueous conditions usually leads to the hydrolysis of the ester bond with only a minor content of the corresponding amide. However, the aminolysis of pentadecanolide (PD) and hexadecanolide (HD), respectively, with oleylamine (OA) in aqueous miniemulsion under optimized conditions (temperature, concentration of enzyme, reaction time) yields >90% amide. Kinetic investigations performed with OA and PD reveal that the lipase catalyzes a novel reaction pathway, i.e., the hydrolysis of a lactone followed by the amidation requiring 30 min and 8 clays reaction time, respectively. The demands of a high amount of lipase as well as the long reaction time are caused by the low reactivity of the carboxylic group and the formation of salt with the amine. Similar reactions were performed with PD and other amines Such as dodecyl, decyl, octyl, benzyl and hexyl amine resulting the analogous amide compounds. (C) 2009 Published by Elsevier B.V.
    DOI:
    10.1016/j.molcatb.2009.11.006
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