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3-phenyl-3-(phenylamino)-1-(p-tolyl)propan-1-one | 801-05-8

中文名称
——
中文别名
——
英文名称
3-phenyl-3-(phenylamino)-1-(p-tolyl)propan-1-one
英文别名
1-(p-methylphenyl)-3-phenyl-3-phenylamino-1-propanone;3-phenyl-3-phenylamino-1-p-tolyl-propan-1-one;3-anilino-3-phenyl-1-p-tolyl-propan-1-one;β-Anilino-4-methyl-β-phenyl-propiophenon;3-Anilino-3-phenyl-1-p-tolyl-propan-1-on;p-Tolyl-(β-anilino-β-phenyl-aethyl)-keton;3-anilino-1-(4-methylphenyl)-3-phenylpropan-1-one
3-phenyl-3-(phenylamino)-1-(p-tolyl)propan-1-one化学式
CAS
801-05-8
化学式
C22H21NO
mdl
——
分子量
315.415
InChiKey
GNOKVQZWFHXTOO-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

物化性质

  • 熔点:
    142 °C
  • 沸点:
    510.0±45.0 °C(Predicted)
  • 密度:
    1.130±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.7
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Pronounced Catalytic Effect of a Micellar Solution of Sodium Dodecylsulfate (SDS) Upon a Three-Component Reaction of Aldehydes, Amines, and Ketones Under Neutral Conditions
    作者:Abbas Ali Jafari、Fatemeh Moradgholi、Fatemeh Tamaddon
    DOI:10.1002/ejoc.200801037
    日期:2009.3
    A micellar solution of anionic, cationic or neutral surfactants can be used as an excellent medium for three-component Mannich reactions of aldehydes, amines, and ketones at room temperature. Sodium dodecylsulfate turned out to efficiently catalyze the reaction in neutral pure water (pH ≈ 7), and the corresponding desired β-amino ketones precipitate while the reactions proceedes. This method provides
    阴离子、阳离子或中性表面活性剂的胶束溶液可用作醛、胺和在室温下进行三组分曼尼希反应的优良介质。结果证明十二烷基硫酸钠在中性纯 (pH ≈ 7) 中有效催化反应,并且在反应进行时相应的所需 β-沉淀。该方法在温和的反应条件、干净的反应曲线、提高的产率和优异的区域选择性和非对映选择性方面提供了一种新的改进的三组分曼尼希反应,后处理简单。观察到在中中性条件下点击化学的有趣例子。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
  • Hf(OTf)4 as a Highly Potent Catalyst for the Synthesis of Mannich Bases under Solvent-Free Conditions
    作者:Shuai-Bo Han、Jing-Ying Wei、Xiao-Chong Peng、Rong Liu、Shan-Shan Gong、Qi Sun
    DOI:10.3390/molecules25020388
    日期:——
    Hf(OTf)4 was identified as a highly potent catalyst (0.1–0.5 mol%) for three-component Mannich reaction under solvent-free conditions. Hf(OTf)4-catalyzed Mannich reaction exhibited excellent regioselectivity and diastereoselectivity when alkyl ketones were employed as substrates. 1H NMR tracing of the H/D exchange reaction of ketones in MeOH-d4 indicated that Hf(OTf)4 could significantly promote the
    Hf(OTf)4 被确定为在无溶剂条件下进行三组分曼尼希反应的高效催化剂(0.1-0.5 mol%)。当使用烷基作为底物时,Hf(OTf)4 催化的曼尼希反应表现出优异的区域选择性和非对映选择性。在 MeOH-d4 中的 H/D 交换反应的 1H NMR 示踪表明 Hf(OTf)4 可以显着促进-醇互变异构化,从而有助于加快反应速率。
  • Mechanistic studies on counter-ionic effects of camphorsulfonate-based ionic liquids on kinetics, thermodynamics and stereoselectivity of β-amino carbonyl compounds
    作者:Sabahat Sardar、Erum Jabeen、Cecilia Devi Wilfred、Ahmad Sazali Hamzah、Jean-Marc Leveque
    DOI:10.1016/j.molliq.2020.114370
    日期:2020.12
    Catalysis is important in various applications of organic chemistry and its output product control for stereoselective compounds is outrageous. Establishment of experimental facts of stereoselective compounds from catalysis and their validation using theoretical evidences is the key to understand various mechanisms of optically active compounds. A family of new ionic liquids (ILs) with various imidazolium
    催化作用在有机化学的各种应用中很重要,其对立体选择化合物的输出产物控制非常苛刻。通过催化作用建立立体选择性化合物的实验事实,并使用理论证据对其进行验证,是理解旋光化合物各种机理的关键。已经合成了具有各种咪唑鎓阳离子和樟脑磺酸根阴离子作为对环境有益的液态盐的一系列新型离子液体(IL),并将其用于催化β-基羰基化合物。使用IL作为均相催化剂形成产物,具有优异的产物收率和非对映选择性。根据反应动力学和产物收率,研究了抗衡离子,IL的哈米特酸度和粘度以及溶剂和温度的影响。密度泛函理论(DFT)用于研究反应机理的热力学研究。DFT计算预测,催化机理涉及IL的两个抗衡离子。此外,有证据表明,合成途径需要较低的活化能,而反途径产生热力学稳定的产物。这项研究探索了使用IL作为潜在的均相催化剂生产立体选择性物质的新途径。
  • H3PW12O40 supported on silica-encapsulated γ-Fe2O3 nanoparticles: a novel magnetically-recoverable catalyst for three-component Mannich-type reactions in water
    作者:Ezzat Rafiee、Sara Eavani
    DOI:10.1039/c1gc15291b
    日期:——
    A new type of magnetically-recoverable catalyst was synthesized by the immobilization of H3PW12O40 on the surface of silica-encapsulated γ-Fe2O3 nanoparticles. This catalyst was characterized by transmission electron microscopy (TEM), a laser particle size analyzer, infrared spectroscopy (IR) and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The results show that the particles are mostly spherical in shape and have an average size of approximately 94 nm. The characterization data derived from IR spectroscopy reveal that H3PW12O40 on the support exists in the Keggin structure. The acidity of the catalyst was measured by a potentiometric titration with n-butylamine. To our surprise, this very strong solid acid catalyst showed an excellent distribution of acid sites, suggesting that the catalyst possesses a higher number of surface active sites compared to its homogeneous analogues. The activity of the catalyst was probed through one-pot three-component Mannich-type reactions of aldehydes, amines and ketones in water at room temperature. The excellent conversions show that the catalyst has strong and sufficient acidic sites, which are responsible for its catalytic performance. After the reaction, the catalyst/product separation could be easily achieved with an external magnetic field, and more than 95% of the catalyst could usually be recovered. The catalyst was reused at least five times without any loss of its high catalytic activity.
    通过将H3PW12O40固定在二氧化硅包覆的γ-Fe2O3纳米颗粒表面,合成了一种新型磁性可回收催化剂。该催化剂通过透射电子显微镜(TEM)、激光粒度分析仪、红外光谱(IR)和电感耦合等离子体原子发射光谱(ICP-AES)进行了表征。结果显示,颗粒主要呈球形,平均尺寸约为94纳米。红外光谱表征数据揭示,负载上的H3PW12O40以Keggin结构存在。催化剂的酸度通过用正丁胺进行的电位滴定法测量。令人惊讶的是,这种非常强的固体酸催化剂显示出优异的酸位点分布,表明催化剂相对于均相类似物具有更高的表面活性位点数量。催化剂的活性通过在中的室温下进行的一锅法三组分Mannich型反应,即醛、胺和的反应来评估。优异的转化率表明,催化剂具有强烈且充分的酸性位点,这是其催化性能的原因。反应后,通过外部磁场可以轻松实现催化剂/产物分离,通常可以回收超过95%的催化剂。该催化剂至少可以重复使用五次,而不会损失其高催化活性。
  • One-pot three-component Mannich-type reaction catalyzed by trifluoromethanesulfonic acid in water
    作者:Gang Li、Hankui Wu、Zhiyong Wang、Xianli Wang
    DOI:10.1134/s0023158411010113
    日期:2011.2
    One-pot three-component Mannich-type reaction of ketones, aldehydes and amines was efficiently catalyzed by liquid trifluoromethanesulfonic acid in water at ambient temperature. The high yield of corresponding β-amino ketones compounds were achieved. The proposed method is mild, green, simple and efficient.
    在环境温度下,液体三氟甲磺酸中能有效地催化,醛和胺的一锅三组分曼尼希型反应。实现了高产率的相应β-化合物。该方法温和,绿色,简单,有效。
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