(5-chloro-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone | 1417412-29-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (5-chloro-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone
• 英文别名: {5-chloro-2-[1-(methoxyimino)ethyl]phenyl}(phenyl)methanone
• CAS: 1417412-29-3
• 化学式: C₁₆H₁₄ClNO₂
• 分子量: 287.746
• InChiKey: SHOOYCCSPJCVHT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.94
• 重原子数：
  20.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  38.66
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为产物：
  描述：

  苯乙酮 在 吡啶 、 selenium(IV) oxide 、 ammonium persulfate 、 palladium diacetate 作用下， 以 二乙二醇二甲醚 为溶剂， 反应 3.0h， 生成 (5-chloro-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone
  参考文献：
  名称：

  Palladium-catalyzed decarboxylative acylation of O-methyl ketoximes with α-keto acids

  摘要：

  描述了一种温和、实用且高效的钯催化脱羧邻位酰基化反应，该反应通过C‒H键活化实现了O-甲基酮肟与α-酮酸的转化。在这些反应中，广泛的O-甲基酮肟和α-酮酸都能以高选择性和良好的耐受性进行脱羧交叉偶联反应。

  DOI：

  10.1039/c2cc38433g

文献信息

• NHPI and palladium cocatalyzed aerobic oxidative acylation of arenes through a radical process
  作者：Yu-Feng Liang、Xiaoyang Wang、Conghui Tang、Tao Shen、Jianzhong Liu、Ning Jiao

  DOI：10.1039/c5cc08945j

  日期：——

  Molecular oxygen, the most environmentally friendly oxidant, was used as the terminal oxidant for palladium-catalyzed radical oxidative acylation of arenes.

  分子氧气，作为最环保的氧化剂，被用作钯催化的芳烃自由基氧化酰化反应的末端氧化剂。
• Palladium-Catalyzed Direct Acylation of Ketoximes and Aldoximes from the Alcohol Oxidation Level through C-H Bond Activation
  作者：Satyasheel Sharma、Minyoung Kim、Jihye Park、Mirim Kim、Jong Hwan Kwak、Young Hoon Jung、Joa Sub Oh、Youngil Lee、In Su Kim

  DOI：10.1002/ejoc.201300649

  日期：2013.10

  A highly efficient palladium-catalyzed oxidative ortho-acylation of O-methyl ketoximes and O-methyl aldoximes with benzylic and aliphatic alcohols from the alcohol oxidation level is described. This protocol potentially provides new opportunities to use readily available alcohols as starting materials for catalytic reactions, and represents a catalytic alternative to transcend the barriers imposed

  描述了一种高效的钯催化氧化邻位酰化 O-甲基酮肟和 O-甲基醛肟与苯甲醇和脂肪醇从醇氧化水平。该协议可能为使用现成的醇作为催化反应的起始材料提供了新的机会，并代表了一种催化替代方案，可以超越经典的弗里德尔-克拉夫茨酰化所施加的障碍。
• Aerobic Oxidation of Pd^II to Pd^IV by Active Radical Reactants: Direct C–H Nitration and Acylation of Arenes via Oxygenation Process with Molecular Oxygen
  作者：Yu-Feng Liang、Xinyao Li、Xiaoyang Wang、Yuepeng Yan、Peng Feng、Ning Jiao

  DOI：10.1021/cs502126n

  日期：2015.3.6

  oxidative C–H nitration and acylation of arenes with simple and readily available tert-butyl nitrite (TBN) and toluene as the radical precursors has been developed. Molecular oxygen is employed as the terminal oxidant and oxygen source to initiate the active radical reactants. Many different directing groups such as pyridine, pyrimidine, pyrazole, pyridol, pyridylketone, oxime, and azo groups can be employed

  已经开发了钯催化的好氧氧化C–H硝化和芳烃与简单易用的亚硝酸叔丁酯（TBN）和甲苯作为自由基前体的酰化反应。分子氧被用作末端氧化剂和氧源以引发活性自由基反应物。在这些新颖的转化中可以使用许多不同的导向基团，例如吡啶，嘧啶，吡唑，吡啶醇，吡啶基酮，肟和偶氮基团。通过自由基过程的Pd II / Pd IV催化循环是这些氧化的CH–H硝化和酰化反应的最可能途径。
• Palladium-Catalyzed Oxidative Direct<i>ortho</i>-C-H Acylation of Arenes with Aldehydes under Aqueous Conditions
  作者：Fuhong Xiao、Shuqing Chen、Huawen Huang、Guo-Jun Deng

  DOI：10.1002/ejoc.201501187

  日期：2015.12

  Palladium-catalyzed ortho-acylation of arenes with aldehydes in the presence of tert-butyl hydroperoxide (TBHP) as the oxidant under aqueous conditions has been demonstrated. The acylation reaction exhibits excellent regioselectivity and wide functional group tolerance.

  钯催化的芳烃与醛在叔丁基过氧化氢 (TBHP) 作为氧化剂的存在下，在水性条件下的邻位酰化已被证明。酰化反应表现出优异的区域选择性和广泛的官能团耐受性。
• Pd-Catalyzed Oxidative Coupling of Arene C–H Bonds with Benzylic Ethers as Acyl Equivalents
  作者：Sangil Han、Satyasheel Sharma、Jihye Park、Mirim Kim、Youngmi Shin、Neeraj Kumar Mishra、Jong Jin Bae、Jong Hwan Kwak、Young Hoon Jung、In Su Kim

  DOI：10.1021/jo4024304

  日期：2014.1.3

  A palladium-catalyzed oxidative coupling of arene C–H bonds with benzylic ethers via C–H bond activation is described. The reaction proceeds efficiently with a broad range of substrates bearing conventional directing groups with excellent functional group compatibility. This protocol potentially provides opportunities to use dibenzyl ethers as new acyl equivalents for catalytic acylation reactions

  描述了芳烃CH键与苄基醚通过CH键活化的钯催化氧化偶联。该反应在带有常规官能团且具有优异官能团相容性的多种底物上有效进行。该方案潜在地提供了使用二苄基醚作为新的酰基等同物进行催化酰化反应的机会。