2-羟基-3-(4-甲基苯基)苯并吡喃-4-酮 | 73791-19-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 中文名称: 2-羟基-3-(4-甲基苯基)苯并吡喃-4-酮
• 英文名称: 4-hydroxy-3-(p-tolyl)-1-benzopyran-2-one
• 英文别名: 4-hydroxy-3-p-tolyl-2H-chromen-2-one；4-hydroxy-3-p-tolylcoumarin；4-hydroxy-3-p-tolyl-chromen-2-one；3-(4-Methylphenyl)-4-hydroxy-cumarin；4-Hydroxy-3-p-tolyl-cumarin；COUMARIN, 4-HYDROXY-3-(p-TOLYL)-；4-hydroxy-3-(4-methylphenyl)chromen-2-one
• CAS: 73791-19-2
• 化学式: C₁₆H₁₂O₃
• 分子量: 252.269
• InChiKey: VFOIMQUAPALECW-UHFFFAOYSA-N

物化性质

• 熔点：
  226 °C
• 沸点：
  451.7±45.0 °C(Predicted)
• 密度：
  1.324±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-羟基-3-(4-甲基苯基)苯并吡喃-4-酮 在 iron(III) chloride 、 silica gel 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 12.0h， 以86%的产率得到9-methyl-6H-benzofuro[3,2-c]chromen-6-one
  参考文献：
  名称：

  FeCl 3介导的4-羟基香豆素的氧化闭环合成Coumestan衍生物

  摘要：

  已经开发了一种简洁有效的方法来合成香豆素类似物。支撑策略涉及FeCl 3介导的4-羟基-3-苯基-2 H-铬烯-2-酮衍生物的分子内直接氧化烯丙基化反应。利用该合成方案，可以容易地从容易获得的试剂中获得多种香豆素衍生物。

  DOI：

  10.1021/jo2000644
• 作为产物：
  描述：

  4-羟基香豆素 在 三叔丁基膦 、 palladium diacetate 、 sodium carbonate 、 lithium hydroxide 作用下， 以 乙二醇二甲醚 、 水 为溶剂， 反应 14.5h， 生成 2-羟基-3-(4-甲基苯基)苯并吡喃-4-酮
  参考文献：
  名称：

  Antitrypanosomal and antioxidant properties of 4-hydroxycoumarins derivatives

  摘要：

  In the present communication we prepared a series of six 4-hydroxycoumarin derivatives, isosters of quercetin, recognized as an antioxidant natural compound, with the aim of evaluating the antitrypanosomal activity against Trypanosoma cruzi, the parasite responsible for Chagas disease, and the antioxidant properties. We have used the 4-hydroxycoumarin moiety (compound 1) as the molecular template for the synthesis of compounds 2-7. These derivates have shown moderate trypanocidal activity. However they have been proved to be good antioxidants. In particular compound 7 is the most active antioxidant and it is, therefore, a potential candidate for a successful employment in conditions characterized by free radicals overproduction. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.07.013

文献信息

• The Rhodium Carbenoid Route to 3-Aryl-4-hydroxycoumarins: Synthesis of Derrusnin
  作者：Stefano Tollari、Giovanni Palmisano、Luca Goldoni、Giancarlo Cravotto、Andrea Penoni

  DOI：10.1055/s-2005-864808

  日期：——

  3-Aryl-4-hydroxycoumarins have been obtained in satisfactory yields and selectivity through a Rh(II)-mediated arylation of diazocoumarin. The utility of this approach is demonstrated by ­synthesis of the natural product derrusnin.

  3-芳基-4-羟基香豆素通过Rh(II)介导的二氮香豆素芳基化反应获得了令人满意的产率和选择性。这种方法的实用性通过天然产物德鲁斯宁的合成得到了证明。
• The chemistry of pentavalent organobismuth reagents
  作者：Derek H.R. Barton、Dervilla M.X. Donnelly、Jean-Pierre Finet、Paul H. Stenson

  DOI：10.1016/s0040-4020(01)89826-4

  日期：——

  The arylation of chroman-4-one and 4-hydroxycoumarin derivatives by pentavalent arylbismuth reagents has been carried out. Chroman-4-one gives the 3-diphenyl derivative, whereas 3-formyl and 3-oxalyl derivatives are phenylated to isoflavanones in moderate to high yields. Arylation of 4-hydroxycoumarins by various Bi(V) reagents gives rise to functionally substituted 3-aryl-4-hydroxycoumarins in high

  已经通过五价芳基铋试剂将苯并二氢吡喃-4-酮和4-羟基香豆素衍生物芳基化。Chroman-4-one生成3-diphenyl衍生物，而3-formyl和3-oxalyl衍生物以中等至高收率被苯基化为异黄酮。通过各种Bi（V）试剂对4-羟基香豆素进行的丙烯酸化反应以高收率产生了功能性取代的3-芳基-4-羟基香豆素。
• Barton, Derek H. R.; Donnelly, Dervilla M. X.; Finet, Jean-Pierre, Journal of the Chemical Society. Perkin transactions I, 1992, p. 1365 - 1376
  作者：Barton, Derek H. R.、Donnelly, Dervilla M. X.、Finet, Jean-Pierre、Guiry, Patrick J.

  DOI：——

  日期：——
• Antitrypanosomal and antioxidant properties of 4-hydroxycoumarins derivatives
  作者：Fernanda Pérez-Cruz、Silvia Serra、Giovanna Delogu、Michel Lapier、Juan Diego Maya、Claudio Olea-Azar、Lourdes Santana、Eugenio Uriarte

  DOI：10.1016/j.bmcl.2012.07.013

  日期：2012.9

  In the present communication we prepared a series of six 4-hydroxycoumarin derivatives, isosters of quercetin, recognized as an antioxidant natural compound, with the aim of evaluating the antitrypanosomal activity against Trypanosoma cruzi, the parasite responsible for Chagas disease, and the antioxidant properties. We have used the 4-hydroxycoumarin moiety (compound 1) as the molecular template for the synthesis of compounds 2-7. These derivates have shown moderate trypanocidal activity. However they have been proved to be good antioxidants. In particular compound 7 is the most active antioxidant and it is, therefore, a potential candidate for a successful employment in conditions characterized by free radicals overproduction. (C) 2012 Elsevier Ltd. All rights reserved.
• Synthesis of Coumestan Derivatives via FeCl₃-Mediated Oxidative Ring Closure of 4-Hydroxy Coumarins
  作者：Lina Tang、Yongle Pang、Qiao Yan、Liuqing Shi、Jianhui Huang、Yunfei Du、Kang Zhao

  DOI：10.1021/jo2000644

  日期：2011.4.15

  A concise and efficient approach to the syntheses of coumestan analogues has been developed. The underpinning strategy involves a FeCl3-mediated direct intramolecular oxidative annellation of 4-hydroxy-3-phenyl-2H-chromen-2-one derivatives. Utilizing this synthetic protocol, a variety of coumestan derivatives were conveniently obtained from readily available reagents.

  已经开发了一种简洁有效的方法来合成香豆素类似物。支撑策略涉及FeCl 3介导的4-羟基-3-苯基-2 H-铬烯-2-酮衍生物的分子内直接氧化烯丙基化反应。利用该合成方案，可以容易地从容易获得的试剂中获得多种香豆素衍生物。