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(E)-n-butyl 3-(2,4-dimethylphenyl)acrylate

中文名称
——
中文别名
——
英文名称
(E)-n-butyl 3-(2,4-dimethylphenyl)acrylate
英文别名
(E)-butyl 3-(2,4-dimethylphenyl)acrylate;butyl (E)-3-(2,4-dimethylphenyl)prop-2-enoate
(E)-n-butyl 3-(2,4-dimethylphenyl)acrylate化学式
CAS
——
化学式
C15H20O2
mdl
——
分子量
232.323
InChiKey
VXJWPIPWVZHEPR-CMDGGOBGSA-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):
    4.2
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    丙烯酸丁酯2,4-二甲基溴苯 在 [1,1'-bis{(S)-4-isopropyloxazolin-2-yl}ferrocene]Pd(II)Cl2 potassium phosphate 作用下, 以 N-甲基吡咯烷酮 为溶剂, 反应 3.0h, 以88%的产率得到(E)-n-butyl 3-(2,4-dimethylphenyl)acrylate
    参考文献:
    名称:
    1,1′-Bis(oxazolinyl)ferrocene-based palladium catalysts: Synthesis, X-ray structures and applications in Suzuki and Heck coupling reactions
    摘要:
    1,1'-Bis(oxazolinyl)ferrocene-based palladium dichloride complexes 2a and 2b were synthesized. X-ray single-crystal diffraction analyses showed that they are of the N,N'-chelating type, and that the coordination mode of 2a, which has an isopropyl group, is of the cis type, whereas that of 2b, which has a tert-butyl group, is the trans one. These two complexes were employed as catalysts for Suzuki and Heck reactions, and showed high catalytic activities in coupling reactions with various aryl halides and counterparts (phenylboronic acid or n-butyl acrylate). Particularly, the catalyst 2a afforded the coupled product of aryl bromide with phenylboronic acid at room temperature. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.12.018
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文献信息

  • Rhodium(II)-Catalyzed Nondirected Oxidative Alkenylation of Arenes: Arene Loading at One Equivalent
    作者:Harit U. Vora、Anthony P. Silvestri、Casper J. Engelin、Jin-Quan Yu
    DOI:10.1002/anie.201310539
    日期:2014.3.3
    bimetallic RhII catalyst promoted the CH alkenylation of simple arenes at 1.0 equivalent without the use of a directing group. A phosphine ligand as well as cooperative reoxidation of RhII with Cu(TFA)2 and V2O5 proved essential in providing monoalkenylated products in good yields and selectivities, especially with di‐ and trisubstituted arenes.
    属的Rh II催化剂促进与c  H在1.0当量,而无需使用定向基团的简单的芳烃的烯基化。膦配体以及Rh II与Cu(TFA)2和V 2 O 5的协同再氧化被证明对于以高收率和选择性提供单烯基化产物至关重要,特别是对于二取代和三取代的芳烃
  • 2-Hydroxy-1,10-phenanthroline vs 1,10-Phenanthroline: Significant Ligand Acceleration Effects in the Palladium-Catalyzed Oxidative Heck Reaction of Arenes
    作者:Cheng-Hao Ying、Shao-Bai Yan、Wei-Liang Duan
    DOI:10.1021/ol4033804
    日期:2014.1.17
    A series of bidentate monoanionic nitrogen ligands were designed and applied in the Pd-catalyzed oxidative Heck reaction of arenes with alkenes. Significant ligand-accelerated effects were observed, and direct C-H functionalized products were formed in high yields with meta-selectivity.
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