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2-(2-chlorobenzoyl)-2-n-propylpentanenitrile | 135664-56-1

中文名称
——
中文别名
——
英文名称
2-(2-chlorobenzoyl)-2-n-propylpentanenitrile
英文别名
2-(2-Chloro-benzoyl)-2-propyl-pentanenitrile;2-(2-chlorobenzoyl)-2-propylpentanenitrile
2-(2-chlorobenzoyl)-2-n-propylpentanenitrile化学式
CAS
135664-56-1
化学式
C15H18ClNO
mdl
——
分子量
263.767
InChiKey
KFYZOEMKDXXBQX-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):
    4.8
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    40.9
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    氰化钠2-Chloro-benzoic acid (1-propyl-butylidene)-hydrazide甲基三辛基氯化铵 air溶剂黄146 作用下, 以 环己烷 为溶剂, 反应 2.0h, 以58%的产率得到2-(2-chlorobenzoyl)-2-n-propylpentanenitrile
    参考文献:
    名称:
    Phase-transfer catalyzed formation of .alpha.-cyano ketones from ketone aroylhydrazones in NaCN(aq)-inert organic solvent system
    摘要:
    Alpha-Cyanoalkyl aryl ketones can be obtained from ketone aroylhydrazones by heterogeneous reaction with aqueous sodium cyanide, an inert organic solvent, and acetic acid in the presence of air and a catalytic amount of a quaternary ammonium salt. The initially formed HCN adducts undergo air oxidation followed by alkaline-induced decomposition affording the alpha-cyanoalkyl ketones. The phase-transfer catalyst promotes all three reactions.
    DOI:
    10.1021/jo00021a038
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文献信息

  • Phase-transfer catalyzed formation of .alpha.-cyano ketones from ketone aroylhydrazones in NaCN(aq)-inert organic solvent system
    作者:Toshiro Chiba、Mitsuhiro Okimoto
    DOI:10.1021/jo00021a038
    日期:1991.10
    Alpha-Cyanoalkyl aryl ketones can be obtained from ketone aroylhydrazones by heterogeneous reaction with aqueous sodium cyanide, an inert organic solvent, and acetic acid in the presence of air and a catalytic amount of a quaternary ammonium salt. The initially formed HCN adducts undergo air oxidation followed by alkaline-induced decomposition affording the alpha-cyanoalkyl ketones. The phase-transfer catalyst promotes all three reactions.
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