5-chloro-2-(pyridin-2-yl)phenyl benzoate | 1186200-30-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 缩酚酸和缩酚酸环醚类
• 英文名称: 5-chloro-2-(pyridin-2-yl)phenyl benzoate
• 英文别名: 2-[(2-benzoyloxy-4-chloro)phenyl]pyridine；(5-Chloro-2-pyridin-2-ylphenyl) benzoate；(5-chloro-2-pyridin-2-ylphenyl) benzoate
• CAS: 1186200-30-5
• 化学式: C₁₈H₁₂ClNO₂
• 分子量: 309.752
• InChiKey: POVOBLSUOMPZCX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  39.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  碘苯二乙酸 在 palladium diacetate 作用下， 以 甲醇 、 1,2-二氯乙烷 、 甲苯 为溶剂， 反应 8.5h， 生成 5-chloro-2-(pyridin-2-yl)phenyl benzoate
  参考文献：
  名称：

  Palladium catalyzed ortho-C–H-benzoxylation of 2-arylpyridines using iodobenzene dibenzoates

  摘要：

  A palladium-catalyzed ortho-C-H-benzoxylation of 2-arylpyridines using iodobenzene dibenzoates has been developed. The reaction employed the stable and easily accessible hypervalent iodine reagents as both benzoxylate source and oxidant which made the protocol simple and facile. It showed high regioselectivity and good functional group tolerance, and gave the mono-benzoxylation products in moderate to excellent yields. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2015.09.097

文献信息

• Copper-catalyzed C–H acyloxylation of 2-phenylpyridine using oxygen as the oxidant
  作者：Feifan Wang、Zhiyang Lin、Weisheng Yu、Qingdong Hu、Chao Shu、Wu Zhang

  DOI：10.1039/c8ra01974f

  日期：——

  o-acyloxylation of 2-phenylpyridine with carboxylic acids using oxygen as the oxidant has been developed. Various acids including aromatic acids, cinnamic acids and aliphatic acids are effective acyloxylation reagents and provide the desired products in moderate to excellent yields. The reaction proceeds well under an oxygen atmosphere, making this method potentially practical.

  已经开发了一种使用氧作为氧化剂的有效的铜催化的 2-苯基吡啶与羧酸的直接邻酰氧基化反应。包括芳香酸、肉桂酸和脂肪酸在内的各种酸是有效的酰氧基化试剂，并以中等至极好的收率提供所需的产品。该反应在氧气气氛下进行得很好，使该方法具有潜在的实用性。
• ‘Ligand-free’ palladium-catalyzed direct C–H bond oxidative acyloxylation of 2-arylpyridines with aromatic carboxylic acids
  作者：Chao-Jun Hu、Xiao-Hong Zhang、Qiu-Ping Ding、Ting Lv、Shao-Peng Ge、Ping Zhong

  DOI：10.1016/j.tetlet.2012.03.022

  日期：2012.5

  A palladium-catalyzed direct C–H bond oxidative acyloxylation of 2-arylpyridines with aromatic carboxylic acids is described. Several 2-arylpyridines derivatives and aromatic carboxylic acids participate in the reaction, providing a series of mono-acyloxylated products in moderate to good yields. Importantly, the reaction can be conducted without using any ligands in a lower temperature.

  描述了2-芳基吡啶与芳族羧酸的钯催化直接CH键氧化酰氧基化反应。几种2-芳基吡啶衍生物和芳族羧酸参与该反应，以中等至良好的产率提供了一系列单酰氧基化的产物。重要的是，可以在较低温度下不使用任何配体的情况下进行反应。
• Cu-catalyzed direct ortho-chlorination/-oxygenation of aryls: Switching of oxidant, control the diversity of products
  作者：Vinayak Botla、Ashok Akudari、Chandrasekharam Malapaka

  DOI：10.1016/j.tetlet.2018.11.071

  日期：2019.1

  Highly regioselective copper catalyzed ortho-chlorination of aryl pyridines was achieved with TBHP as oxidant and 1,2-dichloroethane as chlorinating agent for the first time. Switching the oxidant from TBHP to benzoyl peroxide under identical reaction conditions effects ortho-oxygenation.

  首次以TBHP为氧化剂，以1,2-二氯乙烷为氯化剂，实现了高区域选择性铜催化芳基吡啶的邻氯氯化反应。相同的反应条件下进行开关从TBHP氧化剂到过氧化苯甲酰效果邻-oxygenation。
• Benzylic ethers as arylcarboxy surrogates in substrate directed ortho C–H functionalisation catalysed by copper
  作者：Nilufa Khatun、Arghya Banerjee、Sourav Kumar Santra、Wajid Ali、Bhisma K. Patel

  DOI：10.1039/c5ra03462k

  日期：——

  A copper catalysed o-benzoxylation of 2-arylpyridines has been accomplished using benzylic ethers as the alternative arylcarboxy sources (ArCOO–).

  一种铜催化的2-芳基吡啶的o-苯甲氧基化反应已经成功地利用苄基醚作为替代芳基羧酸源（ArCOO–）。
• Rhodium-Catalyzed <i>ortho</i>-Benzoxylation of sp² C−H Bond
  作者：Zhishi Ye、Wenhui Wang、Fang Luo、Shouhui Zhang、Jiang Cheng

  DOI：10.1021/ol901609t

  日期：2009.9.3

  A rhodium-catalyzed ortho-benzoxylation of the sp(2) C-H bond by carboxylic acids Is described. The procedure tolerates carbomethoxy, formyl, bromo, chloro, and nitro groups, providing the benzoxylated products in moderate to good yields. Importantly, no external oxidant was required for the transformation.