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N-(3-oxo-1,3-diphenylpropyl)benzamide | 91875-49-9

中文名称
——
中文别名
——
英文名称
N-(3-oxo-1,3-diphenylpropyl)benzamide
英文别名
——
N-(3-oxo-1,3-diphenylpropyl)benzamide化学式
CAS
91875-49-9
化学式
C22H19NO2
mdl
——
分子量
329.398
InChiKey
QTBKOGLJPINUKJ-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):
    4
  • 重原子数:
    25
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • VB1–Al2O3-catalyzed one-pot condensation of aromatic ketone, aromatic aldehyde, and amide
    作者:Min Lei、Lei Ma、Lihong Hu
    DOI:10.1016/j.tetlet.2010.07.008
    日期:2010.9
    A novel and green approach for the efficient synthesis of β-amido ketones using VB1–Al2O3 as a heterogeneous catalyst for the first time from an aldehyde, enolizable ketones, and an amide in EtOH is described. The present methodology has several advantages from the economical and environmental points of view, such as simple procedure, low catalyst loading, high atom economy, and good yields.
    描述了一种新颖且绿色的方法,首次使用VB 1 -Al 2 O 3作为多相催化剂从乙醛,可烯化的酮和酰胺在EtOH中有效合成β-酰胺基酮。从经济和环境的观点来看,本方法具有若干优点,例如操作简单,催化剂用量低,原子经济性高和产率高。
  • Synthesis of Mannich type products via a three-component coupling reaction
    作者:Ghanshyam Pandey、Ravi P. Singh、Ashish Garg、Vinod K. Singh
    DOI:10.1016/j.tetlet.2005.01.118
    日期:2005.3
    The reactions of alkyl nitriles, acetyl chloride, aldehydes and β-ketoesters or simple ketones was studied for the one-pot synthesis of β-acetamido carbonyl compounds. It was observed that the reaction proceeds in the absence of Lewis acids. However, a Lewis acid catalyzes the reaction and several were tested. It was found that whereas Cu(OTf)2 is suitable for the coupling of β-ketoesters with aldehydes
    为一锅法合成β-乙酰氨基羰基化合物,研究了烷基腈,乙酰氯,醛和β-酮酸酯或简单酮的反应。观察到反应在不存在路易斯酸的情况下进行。但是,路易斯酸催化该反应,并对其进行了测试。发现Cu(OTf)2适合将β-酮酸酯与醛偶联,而Sc(OTf)3最适合酮。根据中间体的分离和表征,提出了一种可能的机制。
  • One-pot preparation of β-amido ketones/esters in a three-component condensation reaction using magnesium hydrogensulfate as an effective and reusable catalyst
    作者:Hamid Reza Shaterian、Asghar Hosseinian、Majid Ghashang
    DOI:10.1139/v08-013
    日期:2008.5.1
    three-component condensation of an aryl aldehyde, an enolizable ketone or β-keto ester, acetyl chloride, and acetonitrile or benzonitrile in the presence of magnesium hydrogensulfate as an active, recoverable, and reusable green catalyst is described for the synthesis of β-amido ketones/esters at room temperature. The key features of this methodology are simplicity, mild reaction conditions, and high
    在硫酸氢镁作为活性、可回收和可重复使用的绿色催化剂存在下,芳醛、可烯醇化酮或 β-酮酯、乙酰氯和乙腈或苯甲腈的一锅三组分缩合反应被描述用于在室温下合成 β-酰胺酮/酯。该方法的主要特点是简单、反应条件温和、收率高至极好。关键词:多组分反应、硫酸氢镁、多相催化剂、β-酰胺基酮/酯、温和条件。
  • One-Pot Multicomponent Synthesis of β-Acetamido Ketones Based on BiCl<sub>3</sub> Generated in situ from the Procatalyst BiOCl and Acetyl Chloride
    作者:Rina Ghosh、Swarupananda Maiti、Arijit Chakraborty
    DOI:10.1055/s-2004-836024
    日期:——
    Aromatic aldehydes react in one pot at room temperature with enolizable ketones and acetonitrile in the presence of acetyl chloride and catalytic amount of BiOCl producing the corresponding β-acetamido ketones in very high to excellent yields. BiCl3 ­generated in situ from BiOCl and acetyl chloride catalyzes the ­multicomponent reaction.
    芳香醛在室温下一锅反应,与可烯醇化的酮和乙腈在醋酸氯和催化量的BiOCl的存在下,产生对应的β-乙酰氨基酮,产率非常高到优异。BiOCl与醋酸氯原位产生的BiCl3催化了多组分反应。
  • CuSO<sub>4</sub> · 5H<sub>2</sub>O: A Novel, Green, Reusable, and Environmentally Friendly Catalyst for the One-Pot, Four-Component Synthesis of<font>β</font>-Acetamido Carbonyl Compounds
    作者:Farahnaz K. Behbahani、Neda Doragi、Majid M. Heravi
    DOI:10.1080/00397911.2010.529354
    日期:2012.3.1
    Abstract Multicomponent reactions for the synthesis of β-acetamido carbonyl compounds have been gained considerable attention in organic synthesis. In this articles, aromatic aldehydes have been employed in a one-pot reaction with enolizable ketones, acetonitrile, benzonitrile, and acetyl chloride in the presence of copper(II) sulfate petahydrate at ambient temperature to afford the corresponding β-acetamido
    摘要 β-乙酰氨基羰基化合物的多组分反应在有机合成中受到了广泛关注。在这篇文章中,在环境温度下,在五水硫酸铜 (II) 存在下,芳香醛与可烯醇化的酮、乙腈、苄腈和乙酰氯进行一锅反应,得到相应的 β-乙酰氨基酮。产量。报告了新化合物。使用现成的五水硫酸铜 (II) 作为可重复使用和可回收的催化剂,使该过程变得非常简单、方便且环保。图形概要
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