ethyl 2-(4-methylbenzyl)acrylate | 20566-49-8

• 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: ethyl 2-(4-methylbenzyl)acrylate
• 英文别名: Ethyl 2-[(4-methylphenyl)methyl]prop-2-enoate
• CAS: 20566-49-8
• 化学式: C₁₃H₁₆O₂
• 分子量: 204.269
• InChiKey: JZRHSEGPLIXTAA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  ethyl 2-(4-methylbenzyl)acrylate 在 氢氧化钾 、 草酰氯 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 17.0h， 生成 Thiobenzoic acid S-(2-chlorocarbonyl-3-p-tolyl-propyl) ester
  参考文献：
  名称：

  New orally active enkephalinase inhibitors: their synthesis, biological activity, and analgesic properties

  摘要：

  A series of (4S)-4-[(2S)-benzyl-3-mercaptopropionylamino]-4-(N-phenylcarbamoyl)-butyric acids has been identified as potent systemically active enkephalinase inhibitors. Structure-activity relationships (SAR) are discussed. Further chemical modification of the inhibitors was carried out in order to identify the inhibitors which are orally active in an animal model. Compounds of particular interest are the prodrug-like analogues, including 5b (ONO-9902). Their analgesic effects after oral administration were evaluated. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(97)10048-7
• 作为产物：
  描述：

  bis(4-methylphenyl)iodonium trifluoromethanesulfonate 、 ethyl 2-(tosylmethyl)acrylate 在 tetrakis(actonitrile)copper(I) hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 反应 0.5h， 以67%的产率得到ethyl 2-(4-methylbenzyl)acrylate
  参考文献：
  名称：

  铜（I）光催化还原二芳基碘鎓盐形成的芳基自由基：CuII / CuI机制的NMR证据

  摘要：

  通过使用[Cu（dpp）2 ] [PF 6 ]作为光敏复合物和DIPEA作为还原性猝灭剂，实现了对二芳基碘鎓盐的光催化还原。铜催化剂的应用可以在温和的条件下生成芳基，并保持其对CC键形成过程的反应性。

  DOI：

  10.1002/chem.201301449

文献信息

• Pd-Catalyzed Threefold Arylation of Baylis-Hillman Bromides and Acetates with Triarylbismuth Reagents
  作者：Maddali L. N. Rao、Somnath Giri

  DOI：10.1002/ejoc.201200543

  日期：2012.8

  alkyl 2-benzylacrylates and 2-benzylacrylonitriles were synthesized by means of atom-economic cross-couplings of Baylis–Hillman bromides or acetates with BiAr3 under palladium-catalyzed conditions. These reactions, involving threefold aryl couplings using BiAr3 reagents with bromides and acetates, are fast and are completed in 1–2 h with high product yields.

  在钯催化条件下，通过 Baylis-Hillman 溴化物或乙酸盐与 BiAr3 的原子经济交叉偶联合成了功能化的 2-苄基丙烯酸烷基酯和 2-苄基丙烯腈。这些反应涉及使用 BiAr3 试剂与溴化物和乙酸盐进行三重芳基偶联，反应速度快，在 1-2 小时内完成，产品收率高。
• [EN] EP2/4 AGONISTS<br/>[FR] AGONISTES DE EP2/4
  申请人：PFIZER

  公开号：WO2010116270A1

  公开（公告）日：2010-10-14

  EP2/4 compounds having improved dual pharmacological activity are described. The uniqueness of using EP2/4 dual agonists resides in their ability to modify both uveoscleral outflow via the ciliary muscle and conventional outflow via trabecular meshwork and Schlemm's canal all in the same treatment paradigm. The compounds can be employed for the treatment of glaucoma and ocular hypertension. Formula (I).

  描述了具有改进的双重药理活性的EP2/4化合物。使用EP2/4双激动剂的独特之处在于它们能够通过睫状肌修改虹膜房和通过网状层和Schlemm氏管的传统流出，这一切都在同一治疗范式中。这些化合物可用于治疗青光眼和眼压增高。公式（I）。
• Ester-directed orthogonal dual C–H activation and <i>ortho</i> aryl C–H alkenylation <i>via</i> distal weak coordination
  作者：Manickam Bakthadoss、Tadiparthi Thirupathi Reddy、Vishal Agarwal、Duddu S. Sharada

  DOI：10.1039/d1cc06097j

  日期：——

  of two same molecules via dual C–H bond activation in an intermolecular fashion has been developed using a distal ester-directing group. This new coupling reaction led to the synthesis of the highly functionalized 1,3-diaryl molecular architecture in very good yields and with high chemo- and regioselectivities. In addition, using ester as the distal directing group, ortho C–H olefination of α-methyl

  使用远端酯导向基团，通过分子间方式的双 C-H 键活化，在两个相同分子的芳族 C(sp 2 ) 和脂族烯烃 C(sp 2 ) 碳之间进行了前所未有的正交交叉偶联。这种新的偶联反应导致以非常好的收率和高化学和区域选择性合成高度官能化的 1,3-二芳基分子结构。此外，使用酯作为远端导向基团， α-甲基芳基丙烯酸酯和肉桂酸酯与各种烯烃的邻位C-H 烯化反应以非常好的收率和广泛的底物范围实现。
• Ru–Mg promoted reductive cross-coupling of allyl bromides and alkenes to synthesize 1,7-octadienes with an all-carbon quaternary center
  作者：Shurong Zhang、Xinjie Zhao、Guiping Qin

  DOI：10.1039/d4ob00116h

  日期：——

  A Ru-promoted reductive cross-coupling of allyl bromides and electron-deficient alkenes to provide terminal 1,7-octadienes with magnesium as a reductant is reported herein. This approach enables the facile construction of a series of complex terminal 1,7-octadienes with an all-carbon quaternary center under mild reaction conditions, and the synthetic utility of the current method has been demonstrated

  本文报道了钌促进的烯丙基溴和缺电子烯烃的还原交叉偶联，以镁作为还原剂提供末端1,7-辛二烯。该方法能够在温和的反应条件下轻松构建一系列具有全碳四元中心的复杂末端1,7-辛二烯，并且当前方法的合成实用性已通过克级合成得到证明。初步的机制研究表明，这种转变可能不涉及激进途径。
• COMPOUNDS OF CHIRAL AROMATIC SPIROKETAL DIPHOSPHINE LIGANDS, PREPARATION METHODS AND USES THEREOF
  申请人：Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

  公开号：EP2876108B1

  公开（公告）日：2020-09-30