1-((3-bromophenyl)(piperidin-1-yl)methyl)naphthalen-2-ol

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1-((3-bromophenyl)(piperidin-1-yl)methyl)naphthalen-2-ol
• 英文别名: 1-((3-Bromophenyl)(piperidin-1-yl)methyl)naphthalen-2-ol；1-[(3-bromophenyl)-piperidin-1-ylmethyl]naphthalen-2-ol
• 化学式: C₂₂H₂₂BrNO
• 分子量: 396.327
• InChiKey: CKSHACSDKWYAAW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  23.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  哌啶 、 间溴苯甲醛 、 2-萘酚 在 titania-supported perchloric acid 作用下， 反应 0.4h， 以91%的产率得到1-((3-bromophenyl)(piperidin-1-yl)methyl)naphthalen-2-ol
  参考文献：
  名称：

  Nanocrystalline TiO2–HClO4 catalyzed three-component preparation of derivatives of 1-amidoalkyl-2-naphthol, 1-carbamato-alkyl-2-naphthol, 1-(α-aminoalkyl)-2-naphthol, and 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-one

  摘要：

  在催化剂纳米晶 TiO2-HClO4 的存在下，通过 2-萘酚、芳香醛和 NH 化合物（即酰胺、氨基甲酸酯和仲胺）的三组分反应，分别制备了 1-氨基烷基-2-萘酚、1-氨基甲酰基-2-萘酚和 1-(α-氨基烷基)-2-萘酚。此外，在相同的纳米催化剂存在下，通过 2-萘酚、芳香醛和二甲酮的反应，合成了 12-芳基-8,9,10,12-四氢苯并[a]-氧杂蒽-11-酮衍生物。这些反应是在无溶剂条件下进行研究的。这种白色酸性异相催化剂在反应条件下非常稳定，可重复使用多次，且活性无明显下降。

  DOI：

  10.1007/s11164-012-0938-6

文献信息

• Nanocrystalline TiO2–HClO4 catalyzed three-component preparation of derivatives of 1-amidoalkyl-2-naphthol, 1-carbamato-alkyl-2-naphthol, 1-(α-aminoalkyl)-2-naphthol, and 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-one
  作者：Hamid Reza Shaterian、Majid Mohammadnia

  DOI：10.1007/s11164-012-0938-6

  日期：2013.11

  1-Amidoalkyl-2-naphthols, 1-carbamatoalkyl-2-naphthols, and 1-(α-aminoalkyl)-2-naphthols have been prepared by three-component reaction of 2-naphthol, aromatic aldehydes, and NH compounds, i.e. amides, carbamates, and secondary amines, respectively, in the presence of a catalytic amount of nanocrystalline TiO2–HClO4. In addition, 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-one derivatives have been synthesized by reaction of 2-naphthol, aromatic aldehydes, and dimedone in the presence of the same nano catalyst. These reactions were studied under solvent-free conditions. This white acidic heterogeneous catalyst is very stable under the reaction conditions and was reused several times without significant loss of activity.

  在催化剂纳米晶 TiO2-HClO4 的存在下，通过 2-萘酚、芳香醛和 NH 化合物（即酰胺、氨基甲酸酯和仲胺）的三组分反应，分别制备了 1-氨基烷基-2-萘酚、1-氨基甲酰基-2-萘酚和 1-(α-氨基烷基)-2-萘酚。此外，在相同的纳米催化剂存在下，通过 2-萘酚、芳香醛和二甲酮的反应，合成了 12-芳基-8,9,10,12-四氢苯并[a]-氧杂蒽-11-酮衍生物。这些反应是在无溶剂条件下进行研究的。这种白色酸性异相催化剂在反应条件下非常稳定，可重复使用多次，且活性无明显下降。
• Solventless Synthesis of 1-(α-aminoalkyl) Naphthols, Betti Bases, Catalyzed by Nanoparticle Fe₃O₄ at Room Temperature
  作者：Fatemeh Janati、Majid M. Heravi、Ahmad Mir Shokraie

  DOI：10.1080/15533174.2012.762381

  日期：2015.1.2

  A series of 1-(alpha-aminoalkyl) naphthols were synthesized expeditiously in good yields and selectivity from 2-naphthol, alkylamines and aldehydes in the presence of nanoparticle Fe3O4 at room temperature in solvent-free conditions.
• Non-ionic surfactant catalyzed synthesis of Betti base in water
  作者：Atul Kumar、Maneesh Kumar Gupta、Mukesh Kumar

  DOI：10.1016/j.tetlet.2010.01.056

  日期：2010.3

  We have developed an efficient non-ionic surfactant (Triton X-100) catalyzed multicomponent synthesis of Betti base from secondary amine, aromatic aldehydes, and beta-naphthol using Mannich-type reaction in water. Lewis and Bronsted acid catalysts, ionic and non-ionic surfactant have been screened for the reaction. Non-ionic surfactant (Triton X-100) gave the best results and the reaction proceeds through the imine formation, which is stabilized by colloidal dispersion and undergoes nucleophilic addition to afford the corresponding N,N-dialkylated Betti base in excellent yields. (C) 2010 Elsevier Ltd. All rights reserved.
• Synthesis of 1‐aminoalkyl‐2‐naphthols derivatives using an engineered copper‐based nanomagnetic catalyst (Fe ₃ O ₄ @CQD@Si (OEt)(CH ₂ ) ₃ NH@CC@N ₃ @phenylacetylene@Cu)
  作者：Tahereh Akbarpour、Ardeshir Khazaei、Jaber Yousefi Seyf、Negin Sarmasti

  DOI：10.1002/aoc.6361

  日期：2021.10

  present study, a molecular level engineered-based method was used to synthesis a copper-based nanomagnetic catalyst (Fe3O4@CQD@Si (OEt)(CH2)3NH@CC@N3@phenylacetylene@Cu). The as-synthesized catalyst was characterized using different techniques, including infrared (IR), X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM), energy-dispersive

  在本研究中，基于分子水平的工程化方法用于合成铜基纳米磁性催化剂（Fe 3 O 4 @CQD@Si (OEt)(CH 2 ) 3 NH@CC@N 3 @苯基乙炔@Cu） . 使用不同的技术对合成的催化剂进行表征，包括红外（IR）、X 射线粉末衍射（XRD）、场发射扫描电子显微镜（FESEM）和透射电子显微镜（TEM）、能量色散 X 射线光谱（ EDX) 和 EDX 元素映射、感应耦合等离子体 (ICP)、热重分析 (TGA) 和差热分析 (DTA) 以及振动样品磁强计 (VSM)。Fe 3 O 4使用碳量子点 (CQD) 代替传统的 SiO 2保护纳米粒子表面. 在 1-氨基烷基-2-萘酚衍生物的合成中评估了所合成催化剂的活性。反应时间短、反应收率高的无溶剂条件是所制备催化剂的结果。反应如何被催化剂触发由 IR 确定。合成后的催化剂在五个循环后提供了 87.5% 的反应产率。采用傅里叶变换红外