(Z)-ethyl 3-(2-nitrophenyl)acrylate | 94527-24-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: (Z)-ethyl 3-(2-nitrophenyl)acrylate
• 英文别名: 3-(2-nitrophenyl)acrylic acid ethyl ester；ethyl (Z)-3-(2-nitrophenyl)prop-2-enoate
• CAS: 94527-24-9
• 化学式: C₁₁H₁₁NO₄
• 分子量: 221.213
• InChiKey: TYYXOWPEFVCPDV-FPLPWBNLSA-N

物化性质

• 沸点：
  355.3±25.0 °C(Predicted)
• 密度：
  1.237±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (Z)-ethyl 3-(2-nitrophenyl)acrylate 在 水 、 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 4.0h， 以91%的产率得到(Z)-3-(2-nitrophenyl)acrylic acid
  参考文献：
  名称：

  Substituent effects of cis-cinnamic acid analogues as plant growh inhibitors

  摘要：

  1-O-cis-Cinnamoyl-beta-D-glucopyranose is one of the most potent allelochemicals that has been isolated from Spiraea thunbergii Sieb by Hiradate et al. It derives its strong inhibitory activity from cis-cinnamic acid (cis-CA), which is crucial for phytotoxicity. By preparing and assaying a series of cis-CA analogues, it was previously found that the key features of cis-CA for lettuce root growth inhibition are a phenyl ring, cis-configuration of the alkene moiety, and carboxylic acid. On the basis of a structure-activity relationship study, the substituent effects on the aromatic ring of cis-CA were examined by systematic synthesis and the lettuce root growth inhibition assay of a series of cis-CA analogues having substituents on the aromatic ring. While ortho- and para-substituted analogues exhibited low potency in most cases, meta-substitution was not critical for potency, and analogues having a hydrophobic and sterically small substituent were more likely to be potent. Finally, several cis-CA analogues were found to be more potent root growth inhibitors than cis-CA. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.phytochem.2013.08.013
• 作为产物：
  描述：

  邻硝基苯甲醛 、 ethyl 2-[bis(2-isopropylphenoxy)phosphoryl]acetate 在 苄基三甲基氢氧化铵 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 以82%的产率得到(Z)-ethyl 3-(2-nitrophenyl)acrylate
  参考文献：
  名称：

  Substituent effects of cis-cinnamic acid analogues as plant growh inhibitors

  摘要：

  1-O-cis-Cinnamoyl-beta-D-glucopyranose is one of the most potent allelochemicals that has been isolated from Spiraea thunbergii Sieb by Hiradate et al. It derives its strong inhibitory activity from cis-cinnamic acid (cis-CA), which is crucial for phytotoxicity. By preparing and assaying a series of cis-CA analogues, it was previously found that the key features of cis-CA for lettuce root growth inhibition are a phenyl ring, cis-configuration of the alkene moiety, and carboxylic acid. On the basis of a structure-activity relationship study, the substituent effects on the aromatic ring of cis-CA were examined by systematic synthesis and the lettuce root growth inhibition assay of a series of cis-CA analogues having substituents on the aromatic ring. While ortho- and para-substituted analogues exhibited low potency in most cases, meta-substitution was not critical for potency, and analogues having a hydrophobic and sterically small substituent were more likely to be potent. Finally, several cis-CA analogues were found to be more potent root growth inhibitors than cis-CA. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.phytochem.2013.08.013

文献信息

• Amides as precursors of imidoyl radicals in cyclisation reactions
  作者：W. Russell Bowman、Anthony J. Fletcher、Jan M. Pedersen、Peter J. Lovell、Mark R.J. Elsegood、Elena Hernández López、Vickie McKee、Graeme B.S. Potts

  DOI：10.1016/j.tet.2006.10.030

  日期：2007.1

  Amides have been successfully used as precursors of imidoyl radicals for radical cyclisation. The amides have been converted to imidoyl selanides via reaction with phosgene to yield imidoyl chlorides followed by reaction with potassium phenylselanide. Imidoyl selanides were reacted with tributyltin hydride (Bu3SnH) as the radical mediator with triethylborane or AIBN as initiators to yield imidoyl radicals

  酰胺已成功地用作亚胺基自由基的前体，用于自由基环化。酰胺已通过与光气反应生成亚氨酰氯，然后与苯硒化钾反应，已转化为亚氨基酰硒化物。亚胺基硒化物与氢化三丁基锡（Bu 3 SnH）作为自由基介体反应，三乙基硼烷或AIBN作为引发剂，生成亚胺基自由基用于环化反应。酰亚胺基已被环化到烯烃上以产生2，3-取代的吲哚和-喹啉，并且还被吡咯和吲哚上以产生双环和三环杂芳烃。
• The One-Pot Wittig Reaction: A Facile Synthesis of α,β-Unsaturated Esters and Nitriles by Using Nanocrystalline Magnesium Oxide
  作者：Boyapati M. Choudary、Koosam Mahendar、M. Lakshmi Kantam、Kalluri V. S. Ranganath、Taimur Athar

  DOI：10.1002/adsc.200606001

  日期：2006.9

  Nanocrystalline magnesium oxide was found to be an effective heterogeneous, solid base catalyst for the one-pot Wittig reaction to afford α,β-unsaturated esters and nitriles in excellent yields with high E-stereoselectivity in the presence of triphenylphosphine under mild conditions.

  发现纳米晶氧化镁是一种有效的非均相，固态碱催化剂，可在一锅Wittig反应中以温和条件在三苯基膦存在下以高收率和高E-立体选择性以优异的产率提供α，β-不饱和酯和腈。
• Stereoselective Synthesis of Polysubstituted Alkenes through a Phosphine-Mediated Three-Component System of Aldehydes, α-Halo Carbonyl Compounds, and Terminal Alkenes
  作者：Da-Neng Liu、Shi-Kai Tian

  DOI：10.1002/chem.200900177

  日期：2009.4.27

  mediate the one‐pot Wittig reaction of aldehydes with α‐halo carbonyl compounds for the synthesis of 1,2‐disubstituted and trisubstituted alkenes in an excellent stereoselective fashion. Furthermore, the first one‐pot, three‐component reaction of aldehydes, α‐halo acetates, and terminal alkenes has been developed in the presence of PPh3 to produce trisubstituted alkenes with excellent E selectivity (see

  几何控制：PPh 3和丙烯酸甲酯（或丙烯酰胺）能够介导醛与α-卤代羰基化合物的单锅Wittig反应，以出色的立体选择性方式合成1,2-二取代和三取代的烯烃。此外，在PPh 3的存在下，醛，α-卤代乙酸盐和末端烯烃的第一个单锅，三组分反应已经开发出来，可生产具有出色E选择性的三取代烯烃（参见方案）。
• Dual [Fe+Phosphine] Catalysis: Application in Catalytic Wittig Olefination
  作者：Susanne Rommel、Christian Belger、Jeanne-Marie Begouin、Bernd Plietker

  DOI：10.1002/cctc.201500053

  日期：2015.4.20

  Iron hydride complexes of the general formula P2Fe(NO)CO)H are highly active catalysts for the hydrosilylation of aldehydes or ketones and phosphine oxides. Depending on the solvent, the in situ reduction of the phosphine oxide can be faster than the corresponding hydrosilylation of a carbonyl group. This unusual activity was used within the context of catalytic Wittig olefination.

  通式P 2 Fe（NO）CO）H的氢化铁络合物是用于醛或酮和氧化膦的氢化硅烷化的高活性催化剂。取决于溶剂，氧化膦的原位还原可以比羰基的相应氢化硅烷化更快。在催化维蒂希烯化反应中使用了这种不同寻常的活性。
• Regio- and diastereoselective Pd-catalyzed aminochlorocyclization of allylic carbamates: scope, derivatization, and mechanism
  作者：Bruna Papa Spadafora、Francisco Wanderson Moreira Ribeiro、Jullyane Emi Matsushima、Elaine Miho Ariga、Isaac Omari、Priscila Machado Arruda Soares、Diogo de Oliveira-Silva、Elisângela Vinhato、J. Scott McIndoe、Thiago Carita Correra、Alessandro Rodrigues

  DOI：10.1039/d1ob00670c

  日期：——

  diastereoselective synthesis of oxazolidinones via a Pd-catalyzed vicinal C–N/C–Cl bond-forming reaction from internal alkenes of allylic carbamates is reported. The oxazolidinones are obtained in yields of 44 to 95% with high to excellent diastereoselectivities (from 6 : 1 to >20 : 1 dr) from readily available precursors. This process is scalable, and the products are suitable for the synthesis of useful amino

  报道了通过Pd 催化的烯丙基氨基甲酸酯的内部烯烃形成邻位 C-N/C-Cl 键形成恶唑烷酮的区域选择性和非对映选择性合成。从容易获得的前体中以 44 至 95% 的产率获得具有高至优异的非对映选择性（从 6 : 1 到 >20 : 1 dr）的恶唑烷酮。该工艺具有可扩展性，产品适用于合成有用的氨基醇。进行了详细的理论和实验机理研究，以描述该反应通过烯烃的反氨基钯化进行，然后是氧化 C-Pd( II ) 裂解并保留碳立体化学以产生主要的非对映异构体。Cu( Ⅱ )的作用) 在 C-Cl 键形成机制步骤中也被提出。