乙基4-(4-甲氧基苯甲酰基)苯甲酸酯 | 67205-87-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 乙基4-(4-甲氧基苯甲酰基)苯甲酸酯
• 英文名称: 4-(4-methoxy-benzoyl)-benzoic acid ethyl ester
• 英文别名: 4-ethoxycarbonyl-4'-methoxybenzophenone；ethyl 4-(4-methoxybenzoyl)benzoate；4-(4-Methoxybenzoyl)benzoesaeureaethylester；4-Carboethoxy-4'-methoxybenzophenone
• CAS: 67205-87-2
• 化学式: C₁₇H₁₆O₄
• 分子量: 284.312
• InChiKey: NKQLFBJLMAMCGF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  21
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 海关编码：
  2914509090

反应信息

• 作为反应物：
  描述：

  乙基4-(4-甲氧基苯甲酰基)苯甲酸酯 在 palladium on activated charcoal sodium hydroxide 、 氢气 、 三溴化硼 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 4-[4-(4-hydroxybenzyl)benzyl]heptane-3,5-dione
  参考文献：
  名称：

  Antiviral activity of some .beta.-diketones. 4. Benzyl diketones. In vitro activity against both RNA and DNA viruses

  摘要：

  The synthesis and in vitro antiviral evaluation of a series of substituted benzyl beta-diketones are described. The introduction of a styryl group onto the phenyl ring enhanced activity against herpesvirus type 2. The 4-methoxystyryl homologue 8 was evaluated extensively in vitro and was found to be effective against both RNA and DNA viruses. Compound 8 was evaluated in the mouse vagina against herpes simplex type 1 and produced a significant increase in survival rate as well as in survival time.

  DOI：

  10.1021/jm00207a010
• 作为产物：
  描述：

  ethyl 4-(chlorocarbonyl)benzoate 在 iron(III)-acetylacetonate 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 0.5h， 生成 乙基4-(4-甲氧基苯甲酰基)苯甲酸酯
  参考文献：
  名称：

  通过铁催化的芳酰基氰化物的芳基化反应有效合成二芳基酮。

  摘要：

  DOI：

  10.1002/anie.200453696

文献信息

• The Crocacins: Novel Natural Products as Leads for Agricultural Fungicides
  作者：Patrick J. Crowley、Paul A. Worthington、Joe Swanborough、Olivia-Anabelle Sageot、Gordon R. Munns、Ingrid M. Devillers、Christopher R.A. Godfrey、Kevin Gillen、Ian H. Aspinall、John Williams

  DOI：10.2533/000942903777678669

  日期：——

  A short route to the synthesis of analogues of the antifungal but unstable natural product crocacin D was developed. A wide range of compounds were made in which the complex side chain was replaced by simple aromatic units, and many of them showed high activity in a mitochondrial beef heart respiration assay. Some of these compounds were active against plant pathogenic fungi of agricultural importance in glasshouse tests. In order to find compounds with greater stability than the natural crocacins, the photolabile (Z)-enamide was replaced with many different moieties, but none gave rise to useful fungicidal activity.

  一种合成抗真菌但不稳定的天然产物克罗卡辛D类似物的简短路线被开发出来。制造了广泛的化合物，其中复杂的侧链被简单的芳香单元所取代，并且其中许多化合物在牛肉线粒体呼吸试验中显示出高活性。其中一些化合物在温室测试中对农业上重要的植物病原真菌具有活性。为了找到比天然克罗卡辛更稳定的化合物，光敏性的(Z)-酰胺被许多不同的基团所取代，但没有任何一种能产生有用的杀真菌活性。

• Magnesium salt promoted tandem nucleophilic addition–Oppenauer oxidation of aldehydes with organozinc reagents
  作者：Ying Fu、Xing Ling Zhao、Hulmet Hügel、Danfeng Huang、Zhengyin Du、Kehu Wang、Yulai Hu

  DOI：10.1039/c6ob01668e

  日期：——

  A magnesium salt promoted synthesis of ketones via tandem nucleophilic addition–Oppenauer oxidation of aldehydes using organozinc chemistry was demonstrated. Magnesium salts concomitantly generated via magnesium metal mediated organohalide zincation exhibit high efficacy for nucleophilic addition of organozinc reagents to aromatic aldehydes and thereafter Oppenauer oxidation whereby ketones are formed

  证明了镁盐可通过串联亲核加成促进醛的合成-使用有机锌化学对醛进行Oppenauer氧化。通过镁金属介导的有机卤化物锌化同时生成的镁盐具有将有机锌试剂亲核加成到芳族醛中并随后进行Oppenauer氧化的高效率，从而高产率地形成酮。
• Unmasked Acyl Anion Equivalent from Acid Chloride with Indium: Reversed-Polarity Synthesis of Unsymmetric Aryl Aryl and Alkenyl Aryl Ketone through Palladium-Catalyzed Cross-Coupling Reaction
  作者：Dohyung Lee、Taekyu Ryu、Youngchul Park、Phil Ho Lee

  DOI：10.1021/ol500003g

  日期：2014.2.21

  A reversed-polarity synthetic method of a range of unsymmetric aryl aryl and alkenyl aryl ketones has been developed through Pd-catalyzed cross-coupling reaction of acylindium reagents generated in situ from easily available acid chlorides and indium with various electrophiles such as aryl iodide and triflate and alkenyl triflate.

  通过Pd催化从容易获得的酰基氯和铟就地生成的酰基lin试剂与各种亲电试剂（例如碘化芳基和三氟甲磺酸盐）进行钯催化的交叉偶联反应，已开发出了一系列不对称芳基芳基和链烯基芳基酮的反极性合成方法和三氟甲磺酸烯基酯。
• Synthesis of ketones via organolithium addition to acid chlorides using continuous flow chemistry
  作者：Soo-Yeon Moon、Seo-Hee Jung、U. Bin Kim、Won-Suk Kim

  DOI：10.1039/c5ra14890a

  日期：——

  An efficient method for the synthesis of ketones using organolithium and acid chlorides under continuous flow conditions has been developed. In contrast to standard batch chemistry, over-addition of the organolithium to the ketone for the formation of the undesired tertiary alcohol has been minimised representing a direct approach toward ketones.

  已经开发了在连续流动条件下使用有机锂和酰氯合成酮的有效方法。与标准间歇化学相反，已将有机锂过量添加到酮上以形成不希望的叔醇的方法减至最少，这代表了直接制酮的方法。
• Aromatic diketones
  申请人：Sterling Drug Inc.

  公开号：US04153719A1

  公开（公告）日：1979-05-08

  Beta-diketones substituted by an aryl-aliphatic group in which the aliphatic chain is interrupted by a cyclic group, and useful as anti-viral agents, are prepared by interacting the appropriate aryl-aliphatic halide with an alkali metal salt of a beta-diketone.

  通过将适当的芳基-脂肪基卤化物与β-二酮的碱金属盐相互作用，制备了由芳基-脂肪基替代的β-二酮，其中脂肪链被一个环状基团中断，并且这些化合物可用作抗病毒剂。