6-phenyl-3,3-dimethylbenzofuran-2(3H)-one | 1418028-00-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并呋喃
• 英文名称: 6-phenyl-3,3-dimethylbenzofuran-2(3H)-one
• 英文别名: 3,3-Dimethyl-6-phenyl-1-benzofuran-2-one；3,3-dimethyl-6-phenyl-1-benzofuran-2-one
• CAS: 1418028-00-8
• 化学式: C₁₆H₁₄O₂
• 分子量: 238.286
• InChiKey: YOUYVZIZCRYIOB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 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

• 作为产物：
  描述：

  2-([1,1'-biphenyl]-4-yl)-2-methylpropanoic acid 在 碘苯二乙酸 、 potassium acetate 、 palladium diacetate 、 N-乙酰甘氨酸 作用下， 以 叔丁醇 为溶剂， 反应 12.0h， 以88%的产率得到6-phenyl-3,3-dimethylbenzofuran-2(3H)-one
  参考文献：
  名称：

  Pd(II)-Catalyzed Enantioselective C–H Activation/C–O Bond Formation: Synthesis of Chiral Benzofuranones

  摘要：

  Pd(II)-catalyzed enantioselective C-H activation of phenylacetic acids followed by an intramolecular C-O bond formation afforded chiral benzofuranones. This reaction provides the first example of enantioselecctive C-H functionalizations through Pd(II)/Pd(IV) redox catalysis.

  DOI：

  10.1021/ja311259x

文献信息

• Cobalt-catalyzed C H activation/C O formation: Synthesis of benzofuranones
  作者：Abdol R. Hajipour、Zahra Khorsandi

  DOI：10.1016/j.tetlet.2019.151396

  日期：2020.1

  Herein, C-H activation/C-O formation reaction using novel cobalt catalytic system is reported. This reaction was given benzofuranones in moderate to excellent yields at room-temperature under air reaction conditions. The introduced strategy is efficient and low-cost method to synthesized benzofuranones from alpha,alpha-disubstitution acetic acid. (C) 2019 Elsevier Ltd. All rights reserved.
• Direct Lactonization of 2-Arylacetic Acids through Pd(II)-Catalyzed C–H Activation/C–O Formation
  作者：Mingyu Yang、Xingyu Jiang、Wen-Juan Shi、Qi-Lei Zhu、Zhang-Jie Shi

  DOI：10.1021/ol303569b

  日期：2013.2.1

  Palladium-catalyzed direct lactonization of 2-arylacetic acids through a reaction sequence that includes C-H activation/C-O formation is reported. This method provides a concise and efficient pathway to synthesize fully functionalized benzofuranone derivatives, which are highly relevant to bioactive natural and synthetic products.