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N-[(3-nitrophenyl)-(2-hydroxynaphthalen-1-yl)methyl]acrylamide

中文名称
——
中文别名
——
英文名称
N-[(3-nitrophenyl)-(2-hydroxynaphthalen-1-yl)methyl]acrylamide
英文别名
N-[(2-hydroxynaphthalen-1-yl)(3-nitrophenyl)methyl]acrylamide;N-[(2-hydroxynaphthalen-1-yl)-(3-nitrophenyl)methyl]prop-2-enamide
N-[(3-nitrophenyl)-(2-hydroxynaphthalen-1-yl)methyl]acrylamide化学式
CAS
——
化学式
C20H16N2O4
mdl
——
分子量
348.358
InChiKey
NQOJYHAELZNYLE-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):
    4.6
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    95.2
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    间硝基苯甲醛丙烯酰胺2-萘酚三聚氯氰 作用下, 反应 0.33h, 以95%的产率得到N-[(3-nitrophenyl)-(2-hydroxynaphthalen-1-yl)methyl]acrylamide
    参考文献:
    名称:
    在无溶剂条件下由2,4,6-三氯-1,3,5-三嗪催化三组分反应制备酰胺基烷基萘
    摘要:
    摘要描述了酰胺烷基萘的有效的一锅法合成。这涉及2-萘酚,芳族醛和酰胺或脲在催化剂量的2,4,6-三氯-1,3,5-三嗪(TCT,氰尿酰氯)存在下的三组分反应。免费条件。 图形概要
    DOI:
    10.1007/s00706-008-0059-5
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文献信息

  • Highly efficient one-pot three-component Betti reaction in water using reverse zinc oxide micelles as a recoverable and reusable catalyst
    作者:Jie Mou、Gan Gao、Chen Chen、Jie Liu、Jian Gao、Yi Liu、Dongsheng Pei
    DOI:10.1039/c6ra28599f
    日期:——
    Betti bases via a one-pot three-component reaction of 2-naphthol, substituted aldehydes and anilines in aqueous media is reported. Through screening different catalysts, reverse zinc oxide nanomicelles show good activity and high selectivity. The catalyst retained activity after six cycles of reuse and were recoverable. The method has the advantages of atom economy, short reaction time, good yield, and
    的贝提碱基的有效的合成通过2-萘酚的单罐三组分反应,则报告在性介质中被取代的醛和苯胺。通过筛选不同的催化剂,反向氧化锌纳米胶束显示出良好的活性和高选择性。催化剂在重复使用六个循环后仍保持活性,并且是可回收的。该方法具有原子经济,反应时间短,收率高,后处理容易,环保等优点。
  • β-Cyclodextrin-butane sulfonic acid: an efficient and reusable catalyst for the multicomponent synthesis of 1-amidoalkyl-2-naphthols under solvent-free conditions
    作者:Kai Gong、Hualan Wang、Xiaoxue Ren、Ying Wang、Jinghua Chen
    DOI:10.1039/c5gc00384a
    日期:——
    A [small beta]-cyclodextrin-butane sulfonic acid is reported as an efficient catalyst for the one-pot synthesis of 1-amidoalkyl-2-naphthols by the multicomponent condensation of aromatic aldehydes, [small beta]-naphthol and amides under solvent-free conditions. The...
    据报道,小α-环糊精-丁磺酸是在溶剂-溶剂下通过芳香醛,小-萘酚和酰胺的多组分缩合一锅合成1-基烷基-2-的有效催化剂。免费条件。这...
  • Nano Silica Sulfuric Acid an Efficient and Recoverable Heterogeneous Catalyst for the Preparation of Amidoalkyl Naphthols Under Solvent-Free Conditions
    作者:Keivan Ghodrati、Azita Farrokhi、Changiz Karami、Zohre Hamidi
    DOI:10.1080/15533174.2013.809746
    日期:2015.1.2
    An efficient and green method has been developed for the synthesis of amidoalkyl naphthol derivatives through a one-pot three-component condensation of 2-naphthol, aldehydes, and amide in the presence of nano silica sulfuric acid as heterogeneous catalyst under solvent-free conditions.
    在无溶剂条件下,以纳米二氧化硅硫酸为多相催化剂,在2-萘酚,醛和酰胺的一锅式三组分缩合反应中,开发了一种高效的绿色方法,用于合成基烷基萘酚生物
  • A Simple and Efficient Procedure for the Synthesis of Amidoalkyl Naphthols by <i>p</i>-TSA in Solution or under Solvent-Free Conditions
    作者:Mohammad Khodaei、Ahmad Khosropour、Hassan Moghanian
    DOI:10.1055/s-2006-939034
    日期:——
    An efficient and direct procedure for the synthesis of amidoalkyl naphthols has been described that employs a three-component condensation reaction in one pot using aromatic aldehydes, β-naphthol and ureas or amides in the presence of p-toluene sulfonic acid in 1,2-dichloroethane at room temperature or under solvent-free conditions at elevated temperature.
    已经描述了一种用于合成酰基烷基萘酚的有效且直接的方法,该方法在 1,2- 对甲苯磺酸存在下使用芳香醛、β-萘酚或酰胺在一个锅中采用三组分缩合反应。二氯乙烷在室温下或在无溶剂条件下在升高的温度下。
  • Cation‐Exchanged Resins: Efficient Heterogeneous Catalysts for Facile Synthesis of 1‐Amidoalkyl‐2‐naphthols from One‐Pot, Three‐Component Condensations of Amides/Ureas, Aldehydes, and 2‐Naphthol
    作者:Sachin B. Patil、Pankajkumar R. Singh、Mandar P. Surpur、Shriniwas D. Samant
    DOI:10.1080/00397910701263858
    日期:2007.5.1
    Abstract One‐pot, three‐component condensation of 2‐naphthol, amides/ureas, and aldehydes takes place smoothly in the presence of cationexchange resins to afford the corresponding 1‐amidoalkyl‐2‐naphthols in good yield. Indion‐130 is found to be the best catalyst for the reaction and is recyclable. The method is simple, solvent free, and involves a short reaction time.
    摘要 2-萘酚、酰胺/和醛的一锅三组分缩合反应在阳离子交换树脂的存在下顺利进行,以良好的收率得到相应的1-酰胺基烷基-2-萘酚。Indion-130 被发现是该反应的最佳催化剂,并且是可回收的。该方法简单,无溶剂,反应时间短。
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