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1-环戊氧基-4-甲氧基苯 | 65578-69-0

中文名称
1-环戊氧基-4-甲氧基苯
中文别名
——
英文名称
1-(cyclopentyloxy)-4-methoxybenzene
英文别名
1-cyclopentyloxy-4-methoxybenzene
1-环戊氧基-4-甲氧基苯化学式
CAS
65578-69-0
化学式
C12H16O2
mdl
——
分子量
192.258
InChiKey
QHVKHNISZYXMCP-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):
    3.1
  • 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:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4-碘苯甲醚copper(ll) sulfate pentahydratecaesium carbonatesodium ascorbate 、 potassium hydroxide 作用下, 以 二甲基亚砜 为溶剂, 反应 36.5h, 生成 1-环戊氧基-4-甲氧基苯
    参考文献:
    名称:
    Copper and l -sodium ascorbate catalyzed hydroxylation and aryloxylation of aryl halides
    摘要:
    CuSO4 center dot 5H(2)O and NaAsc catalyzed hydroxylation and C-O/C-S cross-coupling reactions of aryl halides with phenols or 4-methylbenzenethiol were described. A wide range of substrates and test cases highlight the synthetic utility of the approach. A series of phenols, diaryl ethers, allcylaryl ethers, and diaryl thioethers were synthesized in high yield. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2015.08.066
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文献信息

  • Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
    申请人:——
    公开号:US20030065187A1
    公开(公告)日:2003-04-03
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及催化的方法,用于在酰胺或胺基团的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在其他实施例中,本发明涉及催化的方法,用于在酰基的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在另一些实施例中,本发明涉及催化的方法,用于在含氮杂环芳烃(例如吲哚吡唑和吲哌)的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在某些实施例中,本发明涉及催化的方法,用于在醇的氧原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氧键。本发明还涉及催化的方法,用于在包含亲核碳原子的反应物(例如烯醇酸盐或丙二酸盐负离子)与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-碳键。重要的是,由于催化剂中的低成本,本发明的所有方法都相对廉价。
  • Simple N-Heterocyclic Carbenes as Ligands in Ullmann-Type Ether and Thioether Formations
    作者:Jiang-Ping Wu、Anjan K. Saha、Nizar Haddad、Carl A. Busacca、Jon C. Lorenz、Heewon Lee、Chris H. Senanayake
    DOI:10.1002/adsc.201600316
    日期:2016.6.16
    A simple N‐heterocyclic carbene (NHC) derived from 1‐methyl‐3‐ethylimidazolium tetrafluoroborate was found to be an efficient ligand for a range of copper‐catalyzed cross‐coupling reactions, leading to the formation of aromatic ethers and thioethers.
    发现一种简单的N-杂环卡宾(NHC)衍生自四硼酸1-甲基-3-乙基咪唑鎓是一系列催化交叉偶联反应的有效配体,导致形成芳族醚和醚。
  • Oxalic Diamides and <i>tert</i>-Butoxide: Two Types of Ligands Enabling Practical Access to Alkyl Aryl Ethers via Cu-Catalyzed Coupling Reaction
    作者:Zhixiang Chen、Yongwen Jiang、Li Zhang、Yinlong Guo、Dawei Ma
    DOI:10.1021/jacs.8b12142
    日期:2019.2.27
    A robust and practical protocol for preparing alkyl aryl ethers has been developed, which relies on using two types of ligands to promote Cu-catalyzed alkoxylation of (hetero)aryl halides. The reaction scope is very general for a variety of coupling partners, particularly for challenging secondary alcohols and (hetero)aryl chlorides. In case of coupling with aryl chlorides and bromides, two oxalic
    已经开发了一种用于制备烷基芳基醚的稳健实用的方案,该方案依赖于使用两种类型的配体来促进 Cu 催化的(杂)芳基卤化物的烷氧基化。反应范围非常适用于各种偶联伙伴,尤其是具有挑战性的仲醇和(杂)芳基。在与芳基化物和化物偶联的情况下,两个草酸二酰胺作为强大的配体叔丁醇首先被证明是催化偶联反应的配体,导致芳基化物在室温下完成烷氧基化。此外,许多碳水化合物生物适用于该偶联反应,以 29-98% 的产率提供相应的碳水化合物-芳基醚。
  • Copper-Catalyzed Coupling of Aryl Iodides with Aliphatic Alcohols
    作者:Martina Wolter、Gero Nordmann、Gabriel E. Job、Stephen L. Buchwald
    DOI:10.1021/ol025548k
    日期:2002.3.1
    and mild method for the coupling of aryl iodides and aliphatic alcohols that does not require the use of alkoxide bases is described. The reactions can be performed in neat alcohol. For more precious alcohols, the etherification was carried out in toluene as solvent using 2 equiv of alcohol. Additionally, the cross-coupling of an optically active benzylic alcohol with an unactivated aryl halide was demonstrated
    [反应:见正文]描述了一种简单而温和的偶联芳基化物和脂肪醇的方法,该方法不需要使用醇盐碱。反应可以在纯醇中进行。对于更珍贵的醇,醚化是在甲苯中作为溶剂,使用2当量的醇进行的。此外,光学活性的苯甲醇与未活化的芳基卤化物的交叉偶联被证明完全保留了构型。
  • <i>N</i>,<i>N</i>-Dimethylglycine-Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Aliphatic Alcohols
    作者:Hui Zhang、Dawei Ma、Weiguo Cao
    DOI:10.1055/s-2007-968010
    日期:2007.2
    The Ullmann-type coupling reactions of aryl iodides and aliphatic alcohols occur at 110 °C with N,N-dimethylglycine as the ligand, giving aryl alkyl ethers in good to excellent yields.
    芳基化物和脂肪醇的 Ullmann 型偶联反应在 110 °C 下发生,N,N-二甲基甘氨酸作为配体,产生了良好到极好的收率的芳基烷基醚。
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