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2-硝基-1,4-二(戊-3-基)苯 | 851385-08-5

中文名称
2-硝基-1,4-二(戊-3-基)苯
中文别名
——
英文名称
1,4-di(1-ethylpropyl)-2-nitrobenzene
英文别名
1-nitro-2,5-di(pentan-3-yl)benzene;Benzene, 1,4-bis(1-ethylpropyl)-2-nitro-;2-nitro-1,4-di(pentan-3-yl)benzene
2-硝基-1,4-二(戊-3-基)苯化学式
CAS
851385-08-5
化学式
C16H25NO2
mdl
——
分子量
263.38
InChiKey
GKRHODSSGQBTLD-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):
    6.2
  • 重原子数:
    19
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    45.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-硝基-1,4-二(戊-3-基)苯 在 Ni (Raney) 一水合肼 作用下, 以 甲醇 为溶剂, 反应 0.12h, 以93%的产率得到2,5-di(1-ethylpropyl)phenylamine
    参考文献:
    名称:
    High intensity ultrasound-assisted reduction of sterically demanding nitroaromatics
    摘要:
    Sterically demanding nitroaromatic compounds have been prepared and reduced to their corresponding amines with high intensity ultrasound using hydrazine in the presence of a Raney nickel catalyst. These reactions were dependent on catalyst quality, solvent and ultrasonic amplitude and, in comparison to their silent reactions, proceeded much faster and afforded higher yields. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.02.038
  • 作为产物:
    描述:
    1,4-二(戊-3-基)苯硝酸 作用下, 以 乙酸酐溶剂黄146 为溶剂, 以48%的产率得到2-硝基-1,4-二(戊-3-基)苯
    参考文献:
    名称:
    High intensity ultrasound-assisted reduction of sterically demanding nitroaromatics
    摘要:
    Sterically demanding nitroaromatic compounds have been prepared and reduced to their corresponding amines with high intensity ultrasound using hydrazine in the presence of a Raney nickel catalyst. These reactions were dependent on catalyst quality, solvent and ultrasonic amplitude and, in comparison to their silent reactions, proceeded much faster and afforded higher yields. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.02.038
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文献信息

  • An Easy Access to Aromatic Azo Compounds under Ultrasound/Microwave Irradiation
    作者:Giancarlo Cravotto、Luisa Boffa、Marco Bia、Werner Bonrath、Massimo Curini、Georgios Heropoulos
    DOI:10.1055/s-2006-951481
    日期:2006.9
    Chemoselective reduction of nitroarenes to azo and azoxy compounds was easily achieved using zinc powder and ­ammonium chloride in DMF or DMF-water (95:5) under high intensity ultrasound (US) or microwave (MW) irradiation, separately or combined. When carried out under conventional heating the reaction required much higher temperatures and gave lower yields. The addition of a small amount of water caused a dramatic increase in the reactivity, permitting the reduction of hindered nitroarenes at the expense of selectivity. A novel reactor for combined US/MW ­irradiation was employed which demonstrated additional beneficial effects.
    利用锌粉和氯化铵在DMF或DMF-水(95:5)中,在高强度超声(US)或微波(MW)辐照下,分别或结合地很容易实现对硝基芳烃的化学选择性还原成偶氮和偶氮氧化物。当在常规加热下进行反应时,需要更高的温度且产率较低。添加少量水显著提高了反应性,使得在牺牲选择性的情况下可以还原受阻的硝基芳烃。采用了一种新型反应器用于联合US/MW辐照,显示出额外的有益效果。
  • High intensity ultrasound-assisted reduction of sterically demanding nitroaromatics
    作者:Georgios A. Heropoulos、Spyros Georgakopoulos、Barry R. Steele
    DOI:10.1016/j.tetlet.2005.02.038
    日期:2005.4
    Sterically demanding nitroaromatic compounds have been prepared and reduced to their corresponding amines with high intensity ultrasound using hydrazine in the presence of a Raney nickel catalyst. These reactions were dependent on catalyst quality, solvent and ultrasonic amplitude and, in comparison to their silent reactions, proceeded much faster and afforded higher yields. (c) 2005 Elsevier Ltd. All rights reserved.
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