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2,2'-(1,2-ethanediyldiimino)-5,5'-dimethylbisphenol | 332371-52-5

中文名称
——
中文别名
——
英文名称
2,2'-(1,2-ethanediyldiimino)-5,5'-dimethylbisphenol
英文别名
2,2'-(1,2-ethanediamine)-5,5'-dimethylbisphenol;2-[2-(2-Hydroxy-4-methylanilino)ethylamino]-5-methylphenol
2,2'-(1,2-ethanediyldiimino)-5,5'-dimethylbisphenol化学式
CAS
332371-52-5
化学式
C16H20N2O2
mdl
——
分子量
272.347
InChiKey
LZUWILAMZRQMCR-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):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    64.5
  • 氢给体数:
    4
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    2,2'-(1,2-ethanediyldiimino)-5,5'-dimethylbisphenol苯硼酸邻二甲苯 为溶剂, 以65%的产率得到N,N'-[1,2-ethane-bis[2-phenyl-(7-methylbenzoxazaborolidine)]]
    参考文献:
    名称:
    Bisoxazaborolidines and boron complexes derived from tetradentate ligands: synthesis and spectroscopic studies
    摘要:
    A series of tetradentate ligands were synthesized and their reaction with arylboronic acids was studied. Two classes of tetradentate ligands are discussed, which are mainly based on ONNO and ONOO donor sets and involve 2-aminophenol derivatives and Schiff bases. The reaction of phenylboronic acid with tetradentate ligands derived from 2-aminophenol leads to bisoxazaborolidines containing five-membered rings formed by CCNBO atoms, where the boron atoms have a trigonal geometry. In contrast, tetradentate ligands derived from Schiff bases lead to monomeric and dimeric boron complexes, in which the boron atoms have a tetrahedral geometry stabilized by an intramolecular N-B dative bond. The structures of two boron compounds were established by X-ray diffraction analysis. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2004.02.018
  • 作为产物:
    描述:
    6-氨基间甲酚硼烷 作用下, 以 四氢呋喃 为溶剂, 反应 8.0h, 生成 2,2'-(1,2-ethanediyldiimino)-5,5'-dimethylbisphenol
    参考文献:
    名称:
    由2,2'-(1,2-乙二基二亚氨基)双酚轻松合成1,3,6-氧杂二氮杂卓
    摘要:
    描述了用于合成包括恶二氮杂环的各种杂环系统的有用的反应序列。关键步骤涉及取代的2,2'-(1,2-乙二基二亚氨基)双酚与乙二醛的缩合反应,以立体选择性地提供6a,7a-trans-6,6a,7a,8,15,16-六氢[1,4] X射线衍射确定的]苯并恶嗪[4',3':6,7] [1,3,6]恶二氮杂环庚烷[2,3- c ] [1,4]-苯并恶嗪-6,8-二醇骨架分析。
    DOI:
    10.1016/s0040-4020(00)00984-4
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文献信息

  • 13C NMR spectral assignment of 1,4-diarylpiperazinones
    作者:Arturo Abreu、Ma. Eugenia Ochoa、Norberto Farfán、Rosa Santillan
    DOI:10.1002/mrc.1717
    日期:2006.1
    describes the preparation of a series of new 1,4‐diarylsubstituted‐2‐piperazinones by condensation of substituted N,N′‐bis‐(2‐hydroxyphenyl)‐ethylenediamines with glyoxal and the complete 13C NMR spectral assignment accomplished using APT, HMQC and HMBC techniques. Substituent chemical‐shift effects (SCS) were calculated, which showed different values for the lactam‐ and amine‐substituted aromatic rings
    哌嗪酮衍生物在医药、高分子和纺织领域具有潜在的应用价值。本工作描述了通过取代的 N,N'-双-(2-羟基苯基)-乙二胺与乙二醛缩合制备一系列新的 1,4-二芳基取代-2-哌嗪酮,并使用 APT 完成了完整的 13C NMR 光谱分配, HMQC 和 HMBC 技术。计算了取代基化学位移效应(SCS),表明内酰胺和胺取代的芳环具有不同的值。结果表明,由于电子和空间效应,基于 SCS 效应的预测对于这些分子并不简单。此外,在邻位取代衍生物 2 g 的情况下,NMR 光谱揭示了与苯基旋转受限(阻转异构)相关的动态行为。
  • Facile synthesis of 1,3,6-oxadiazepines from 2,2′-(1,2-ethanediyldiimino)bisphenols
    作者:Ma.Eugenia Ochoa、Susana Rojas-Lima、Herbert Höpfl、Patricia Rodrı́guez、Dolores Castillo、Norberto Farfán、Rosa Santillan
    DOI:10.1016/s0040-4020(00)00984-4
    日期:2001.1
    A useful sequence of reactions for the syntheses of a variety of heterocyclic systems including an oxadiazepine ring is described. The key step involves the condensation of substituted 2,2′-(1,2-ethanediyldiimino)bisphenols with ethanedial to provide stereoselectively the 6a,7a-trans-6,6a,7a,8,15,16-hexahydro[1,4]benzoxazine[4′,3′:6,7][1,3,6]oxadiazepino[2,3-c][1,4]-benzoxazine-6,8-diol framework,
    描述了用于合成包括恶二氮杂环的各种杂环系统的有用的反应序列。关键步骤涉及取代的2,2'-(1,2-乙二基二亚氨基)双酚与乙二醛的缩合反应,以立体选择性地提供6a,7a-trans-6,6a,7a,8,15,16-六氢[1,4] X射线衍射确定的]苯并恶嗪[4',3':6,7] [1,3,6]恶二氮杂环庚烷[2,3- c ] [1,4]-苯并恶嗪-6,8-二醇骨架分析。
  • Bisoxazaborolidines and boron complexes derived from tetradentate ligands: synthesis and spectroscopic studies
    作者:Victor Barba、Alejandro Rodrı́guez、Ma Eugenia Ochoa、Rosa Santillan、Norberto Farfán
    DOI:10.1016/j.ica.2004.02.018
    日期:2004.7
    A series of tetradentate ligands were synthesized and their reaction with arylboronic acids was studied. Two classes of tetradentate ligands are discussed, which are mainly based on ONNO and ONOO donor sets and involve 2-aminophenol derivatives and Schiff bases. The reaction of phenylboronic acid with tetradentate ligands derived from 2-aminophenol leads to bisoxazaborolidines containing five-membered rings formed by CCNBO atoms, where the boron atoms have a trigonal geometry. In contrast, tetradentate ligands derived from Schiff bases lead to monomeric and dimeric boron complexes, in which the boron atoms have a tetrahedral geometry stabilized by an intramolecular N-B dative bond. The structures of two boron compounds were established by X-ray diffraction analysis. (C) 2004 Elsevier B.V. All rights reserved.
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