摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(4-methoxyphenyl)-4-phenyl-1-p-tolyl-1H-imidazole | 412916-85-9

中文名称
——
中文别名
——
英文名称
2-(4-methoxyphenyl)-4-phenyl-1-p-tolyl-1H-imidazole
英文别名
2-(4-Methoxyphenyl)-1-(4-methylphenyl)-4-phenylimidazole
2-(4-methoxyphenyl)-4-phenyl-1-p-tolyl-1H-imidazole化学式
CAS
412916-85-9
化学式
C23H20N2O
mdl
——
分子量
340.425
InChiKey
RENFFJHNLSWCTF-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

物化性质

  • 熔点:
    122-123 °C(Solv: ethanol (64-17-5); water (7732-18-5))
  • 沸点:
    549.1±60.0 °C(Predicted)
  • 密度:
    1.10±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.3
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    27
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    二甲基亚砜 为溶剂, 反应 20.0h, 以100%的产率得到2-(4-methoxyphenyl)-4-phenyl-1-p-tolyl-1H-imidazole
    参考文献:
    名称:
    四氢咪唑并[1,5 - b ]异恶唑-2,3-二羧酸酯的热重排。3 H-咪唑-1-鎓烷基化物及其银衍生物的合成
    摘要:
    异恶唑啉2从咪唑啉-3-氧化物环加成1与DMAD经历重排,以3,4-二氢-2- ħ咪唑-1-鎓-1-(1,2-双-甲氧基羰基-2-氧代ethanides)3,当在甲苯中加热回流时,其自发消除,得到3 H-咪唑-1-鎓-1-(1,2-双-甲氧基羰基-2-氧代乙烷)5或1 H-咪唑6。C-6上芳环的存在降低了转化率,并提高了5的收率。极性比甲苯强的溶剂(例如DMSO)可实现2到6的定量转化在温和条件下,而在极性较小的溶剂(如CCl 4)中,反应速率降低,5的收率提高。C-2未取代的内鎓盐5用银处理过的2 O或硝酸银3中的的Et存在下3 Ñ在室温下,得到C-2的金属化衍生物9在良好的产率。
    DOI:
    10.1016/j.tet.2010.01.037
点击查看最新优质反应信息

文献信息

  • Iron(III)-catalyzed synthesis of multi-substituted imidazoles via [3+2] cycloaddition reaction of nitroolefins and N-aryl benzamidines
    作者:Xiang Liu、Dong Wang、Baohua Chen
    DOI:10.1016/j.tet.2013.08.077
    日期:2013.11
    A novel and efficient iron(III)-catalyzed synthesis of multi-substituted imidazoles via [3+2] cycloaddition of nitroolefins and N-aryl benzamidines under the air atmosphere had been developed. This methodology is convenient, atom-economical, general, and eco-friendly in good yields and prefect regioselectivities.
    多取代的咪唑的通过一种新颖的和有效的(III)催化的合成[3 + 2] nitroolefins和环加成Ñ的空气气氛下,芳基苯甲脒已经被开发出来。这种方法很方便,原子经济性,一般情况下,在良好的收益率和完善的区域选择性环保。
  • Synthesis of Multisubstituted Imidazoles via Copper-Catalyzed [3 + 2] Cycloadditions
    作者:Dong Tang、Ping Wu、Xiang Liu、Yong-Xin Chen、Shuai-Bo Guo、Wen-Lin Chen、Jia-Gen Li、Bao-Hua Chen
    DOI:10.1021/jo302555z
    日期:2013.3.15
    A simple route for the synthesis of imidazole derivatives via copper-catalyzed [3 + 2] cycloaddition reaction is described. This strategy has achieved high regioselectivity and used oxygen as an oxidant without the addition of expensive catalysts to provide moderate to good yields.
    描述了通过催化的[3 + 2]环加成反应合成咪唑生物的简单途径。该策略已实现了较高的区域选择性,并使用氧气作为氧化剂,而无需添加昂贵的催化剂以提供中等至良好的收率。
  • I<sub>2</sub>-Catalyzed diamination of acetyl-compounds for the synthesis of multi-substituted imidazoles
    作者:Jinpeng Qu、Ping Wu、Dong Tang、Xu Meng、Yongxin Chen、Shuaibo Guo、Baohua Chen
    DOI:10.1039/c5nj00910c
    日期:——

    We have successfully developed the I2-catalysed synthesis of substituted imidazole derivatives from amidines and ketones in good to excellent yields and 100% regioselectivity.

    我们已成功开发出I2催化的合成方法,用于从酰胺和酮中制备取代咪唑生物,产率良好至极佳,且100%选择性。
  • Copper and zinc co-catalyzed synthesis of imidazoles via the activation of sp3 C–H and N–H bonds
    作者:Dong Tang、Xiao-Long Li、Xin Guo、Ping Wu、Ji-Hui Li、Kai Wang、Huan-Wang Jing、Bao-Hua Chen
    DOI:10.1016/j.tet.2014.04.054
    日期:2014.7
    An efficient and facile approach to synthesize imidazoles from amidines and arylketone via oxidative coupling of sp(3) C-H bond and N-H bond is reported. This strategy exhibits high performance in terms of regioselectivity with moderate to high yields by using easily available materials, and provides an alternative method to synthesize multi-substituted imidazole skeletons. (C) 2014 Elsevier Ltd. All rights reserved.
  • Iron(III)-Catalyzed Synthesis of 1,2,4-Trisubstituted Imidazoles through the Reactions of Amidines and Aldehydes in Air
    作者:Xiang Liu、Dong Wang、Yongxin Chen、Dong Tang、Baohua Chen
    DOI:10.1002/adsc.201300590
    日期:2013.10.11
    AbstractA novel and efficient iron(III)‐catalyzed synthesis of 1,2,4‐trisubstituted imidazoles through the reactions of amidines and aldehydes in air has been developed. Five hydrogen dissociations involving CH and NH bond activation are realized under mild conditions in this approach. The procedure is sustainable, simple and environmentally friendly.magnified image
查看更多