7-甲基-4-苯基-3,4-二氢色烯-2-酮 | 88407-29-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 新黄酮类化合物
• 中文名称: 7-甲基-4-苯基-3,4-二氢色烯-2-酮
• 英文名称: 3,4-dihydro-7-methyl-4-phenyl-2H-1-benzopyran-2-one
• 英文别名: 7-methyl-4-phenyl-3,4-dihydrobenzopyran-2-one；7-methyl-4-phenyl-3,4-dihydrocoumarin；7-methyl-4-phenylchroman-2-one；7-methyl-4-phenyl-chroman-2-one；7-Methyl-4-phenyl-chroman-2-on；7-Methyl-4-phenyl-3,4-dihydrochromen-2-one
• CAS: 88407-29-8
• 化学式: C₁₆H₁₄O₂
• 分子量: 238.286
• InChiKey: DVIONHZDAYXRBA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  7-甲基-4-苯基-3,4-二氢色烯-2-酮 在 sodium hydroxide 、 LiAlH4 、 potassium carbonate 作用下， 以 甲醇 、 水 、 丙酮 为溶剂， 生成 3-(2-Methoxy-4-methylphenyl)-3-phenylpropanol
  参考文献：
  名称：

  New amines, their use and preparation

  摘要：

  公开号：

  EP0325571B1
• 作为产物：
  描述：

  3-甲基苯基肉桂酸酯 在 硫酸 作用下， 生成 7-甲基-4-苯基-3,4-二氢色烯-2-酮
  参考文献：
  名称：

  Simpson; Israelstam, Journal of the South African Chemical Institute, 2 <1949> 165, 168, 169

  摘要：

  DOI：

文献信息

• p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions
  作者：Arun R. Jagdale、Arumugam Sudalai

  DOI：10.1016/j.tetlet.2007.05.059

  日期：2007.7

  Hydroarylation of cinnamic acids with anisoles and phenols mediated by p-toluenesulfonic acid (p-TSA) under metal and solvent-free conditions gave 3-(4-methoxyphenyl)-3-phenylpropanoic acids and dihydrocoumarins, respectively, in high yields and excellent selectivity.

  在无金属和无溶剂条件下，对甲苯磺酸（p -TSA）介导的肉桂酸与茴香醚和苯酚的氢芳基化反应分别获得了3-（4-甲氧基苯基）-3-苯基丙酸和二氢香豆素，具有高收率和优异的选择性。
• Selective Synthesis of 3,4-Dihydrocoumarins and Chalcones from Substituted Aryl Cinnamic Esters
  作者：Jae-Ho Jeon、Deok-Mo Yang、Jong-Gab Jun

  DOI：10.5012/bkcs.2011.32.1.65

  日期：2011.1.20

  Coumarins are ubiquitous in plant kingdom and have been used as antitumor, antifungals, anticoagulants, insecticides. Chalcones are also widespread in plant kingdom and have been known to possess diverse biological activities; antibacterial, antifungal, antitumor and anti-inflammatory, etc. As they are considered as important natural products, numerous synthetic approaches have been reported up to the present. We devise a new selective method of preparing dihydrocoumarins and chalcones from aryl cinnamates by the selection of reagents. Dihydrocoumarin derivatives were prepared selectively by using intramolecular cyclization catalyzed by p-toluene sulfonic acid. Also, chalcones were prepared by Fries-rearrangement catalyzed by $TiCl_4$. This method can be used for preparing various coumarin & chalcone compounds.

  香豆素广泛存在于植物王国中，并已被用作抗癌剂、抗真菌剂、抗凝血剂和杀虫剂。查尔酮也在植物王国中广泛分布，并且已知具有多种生物活性，包括抗菌、抗真菌、抗癌和抗炎等。由于它们被认为是重要的天然产物，迄今为止已经报道了许多合成方法。我们设计了一种新的选择性方法，通过选择试剂，从芳基肉桂酸制备二氢香豆素和查尔酮。通过使用对甲苯磺酸催化的分子内环化反应，选择性地制备了二氢香豆素衍生物。此外，还通过三氯化钛催化的Fries重排反应制备了查尔酮。这种方法可以用于制备各种香豆素和查尔酮化合物。
• 3,3-diphenylpropylamines and pharmaceutical compositions thereof
  申请人：Pharmacia Aktiebolag

  公开号：US05382600A1

  公开（公告）日：1995-01-17

  ##STR1## Novel 3,3-diphenylpropylamines of formula (I) wherein R.sup.1 signifies hydrogen or methyl, R.sup.2, R.sup.3 and R.sup.4 independently signify hydrogen, methyl, methoxy, hydroxy, carbamoyl, sulphanoyl or halogen, and X represents a tertiary amino group -NR.sup.5, R.sup.6, wherein R.sup.5 and R.sup.6 signify non-aromatic hydrocarbyl groups, which may be the same or different and which together contain at least three carbon atoms, and which may form a ring together with the amine nitrogen, their salts with physiologically acceptable acids and, when the compounds can be in the form of optical isomers, the racemic mixture and the individual enantiomers, their use as drugs, especially as anticholinergic agents, their use for preparing an anticholinergic drug, pharmaceutical compositions containing the novel amines, and methods for preparing the same.

  式（I）的新型3,3-二苯基丙胺化合物，其中R.sup.1表示氢或甲基，R.sup.2、R.sup.3和R.sup.4独立表示氢、甲基、甲氧基、羟基、氨基甲酰基、磺酰基或卤素，X代表三级氨基-NR.sup.5，R.sup.6，其中R.sup.5和R.sup.6表示非芳香烃基，可以相同也可以不同，并且总共含有至少三个碳原子，它们可以与胺氮形成环，它们与生理上可接受的酸盐，当化合物可以是光学异构体时，它们的消旋混合物和单体对映体，它们作为药物的用途，特别是作为抗胆碱能药物的用途，它们用于制备抗胆碱能药物，含有新型胺的药物制剂，以及其制备方法。
• Lewis acid promoted dual bond formation: facile synthesis of dihydrocoumarins and spiro-tetracyclic dihydrocoumarins
  作者：Pedireddi Niharika、Bokka Venkat Ramulu、Gedu Satyanarayana

  DOI：10.1039/c4ob00490f

  日期：——

  Lewis acid (FeCl3) mediated dual bond (C–C and C–O) formation for synthesis of 3,4-dihydrocoumarins is presented. This method has successfully delivered a number of dihydrocoumarins containing dense functionalities on the aromatic ring. Significantly, the present method enabled achieving dihydrocoumarins with tertiary as well as quaternary carbon atoms at the benzylic position. Gratifyingly, the novel spiro-tetracyclic lactones have also been dextrously prepared using this process.

  介绍了一种以路易斯酸（FeCl3）为媒介的双键（C–C 和 C–O）形成方法，用于合成3,4-二氢香豆素。这种方法成功地合成了多种在芳香环上含有密集功能团的二氢香豆素。值得注意的是，这种方法能够实现含有三级和四级碳原子的苯乙基位置的二氢香豆素。此外，采用此工艺还巧妙地制备了新型的螺环四环内酯。
• Solvent-free synthesis of 4-aryl-3,4-dihydrobenzopyran-2-ones via [3+3] cyclocoupling of phenols with cinnamic acid catalyzed by molecular iodine
  作者：Durga P. Kamat、Santosh G. Tilve、Vijayendra P. Kamat

  DOI：10.1016/j.tetlet.2012.06.069

  日期：2012.8

  Molecular iodine was used as a catalyst in the [3+3] cyclocoupling of phenols and cinnamic acids which proceeds via a tandem esterification–hydroarylation process at 120–130 °C under solvent-free conditions. Substituted 4-aryl-3,4-dihydrobenzopyran-2-ones were obtained in good yields.

  分子碘被用作苯酚和肉桂酸的[3 + 3]环偶联反应的催化剂，该过程在无溶剂条件下通过串联酯化-氢芳基化过程在120-130°C下进行。以高收率获得了取代的4-芳基-3,4-二氢苯并吡喃-2-酮。