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4-Methoxy-N-methyl-2-(2-methylcyclopropyl)benzenamine | 1004968-24-4

中文名称
——
中文别名
——
英文名称
4-Methoxy-N-methyl-2-(2-methylcyclopropyl)benzenamine
英文别名
4-methoxy-N-methyl-2-(2-methylcyclopropyl)aniline
4-Methoxy-N-methyl-2-(2-methylcyclopropyl)benzenamine化学式
CAS
1004968-24-4
化学式
C12H17NO
mdl
——
分子量
191.273
InChiKey
ZYAYDAUTSDZDJG-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):
    3
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    N-甲基-P-氨基苯甲醚正丁基锂 作用下, 以 四氢呋喃 为溶剂, 以25%的产率得到
    参考文献:
    名称:
    The first example of direct cyclopropylation of arylamines at the 2-position with magnesium cyclopropylidenes
    摘要:
    Treatment of magnesium cyclopropylidenes, which were generated from 1-chlorocyclopropyl phenyl sulfoxides with isopropylmagnesium chloride in THF at -78 degrees C, with N-lithio arylamines gave arylamines cyclopropylated at the 2-position in moderate to good yields. Use of the magnesium cyclopropylidenes having at least one substituent was found to be essential to this cyclopropylation. This procedure offers a novel synthesis of arylamines having a cyclopropane ring at the 2-position directly from arylamines. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.10.122
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文献信息

  • The first example of direct cyclopropylation of arylamines at the 2-position with magnesium cyclopropylidenes
    作者:Yukie Yamada、Mariko Miura、Tsuyoshi Satoh
    DOI:10.1016/j.tetlet.2007.10.122
    日期:2008.1
    Treatment of magnesium cyclopropylidenes, which were generated from 1-chlorocyclopropyl phenyl sulfoxides with isopropylmagnesium chloride in THF at -78 degrees C, with N-lithio arylamines gave arylamines cyclopropylated at the 2-position in moderate to good yields. Use of the magnesium cyclopropylidenes having at least one substituent was found to be essential to this cyclopropylation. This procedure offers a novel synthesis of arylamines having a cyclopropane ring at the 2-position directly from arylamines. (c) 2007 Elsevier Ltd. All rights reserved.
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