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(Z)-ethyl 3-(2-chlorophenyl)acrylate

中文名称
——
中文别名
——
英文名称
(Z)-ethyl 3-(2-chlorophenyl)acrylate
英文别名
ethyl (Z)-3-(2-chlorophenyl)prop-2-enoate;ethyl 3-(2-chlorophenyl)acrylate
(Z)-ethyl 3-(2-chlorophenyl)acrylate化学式
CAS
——
化学式
C11H11ClO2
mdl
——
分子量
210.66
InChiKey
ILTRCHMHGZQVGO-FPLPWBNLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    14
  • 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:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (Z)-ethyl 3-(2-chlorophenyl)acrylate 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以77%的产率得到cis-o-Chlor-zimtsaeure
    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:
    2-氯苯甲醛ethyl 2-[bis(2-isopropylphenoxy)phosphoryl]acetate苄基三甲基氢氧化铵 作用下, 以 四氢呋喃甲醇 为溶剂, 以90%的产率得到(Z)-ethyl 3-(2-chlorophenyl)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
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文献信息

  • One-Pot Synthesis of α,β-Unsaturated Esters, Ketones, and Nitriles from Alcohols and Phosphonium Salts
    作者:Xiaochun Yu、Shun Wang、Weijie Ding、Juan Hu、Huile Jin
    DOI:10.1055/s-0036-1590904
    日期:2018.1
    reacted not only with benzylic and heteroaromatic alcohols, but also with aliphatic alcohols, forming the corresponding α,β-unsaturated esters, ketones, and nitriles in moderate to excellent yields. A general method for the synthesis of α,β-unsaturated esters, ketones, and nitriles is successfully achieved by a one-pot copper-catalyzed oxidation with O2 in air as oxidant. The solvent mixture of acetonitrile
    摘要 通过在空气中以O 2为氧化剂的一锅铜催化氧化成功地实现了合成α,β-不饱和酯,酮和腈的通用方法。乙腈和甲酰胺(1:1)的溶剂混合物经过优化,可确保在一锅中有效地进行醇类的氧化,de盐的去质子化和Wittig反应。已针对该方法探索了广泛的底物,包括三个吸电子基团(CO 2 Et,COPh,CN)官能化的salts盐。它们不仅与苄基和杂芳族醇反应,而且与脂族醇反应,以中等至极好的收率形成相应的α,β-不饱和酯,酮和腈。 通过在空气中以O 2为氧化剂的一锅铜催化氧化成功地实现了合成α,β-不饱和酯,酮和腈的通用方法。乙腈和甲酰胺(1:1)的溶剂混合物经过优化,可确保在一锅中有效地进行醇类的氧化,de盐的去质子化和Wittig反应。已针对该方法探索了广泛的底物,包括三个吸电子基团(CO 2 Et,COPh,CN)官能化的salts盐。它们不仅与苄基和杂芳族醇反应,而且与脂族醇反应,以中等至极
  • Facile synthesis of α, β-unsaturated esters through a one-pot copper-catalyzed aerobic oxidation-Wittig reaction
    作者:Cheng Ren、Zhenyu Shi、Weijie Ding、Zhiqing Liu、Huile Jin、Xiaochun Yu、Shun Wang
    DOI:10.1016/j.tetlet.2017.09.020
    日期:2018.1
    An efficient one-pot synthesis of α, β-unsaturated esters through the aerobic oxidation – Wittig tandem reaction of alcohols and phosphorous ylide is developed. This new method operates under mild reaction conditions, and uses CuI/TEMPO (TEMPO = 2,2,6,6-tetramethylpiperidine-N-oxyl) as co-catalyst and air (O2) as the oxidant. It tolerates a wide range of functionalized benzylic alcohol and aliphatic
    开发了一种有效的一锅法合成α,β-不饱和酯的方法,即通过醇与磷的叶立德的好氧氧化-Wittig串联反应。该新方法在温和的反应条件下运行,并使用CuI / TEMPO(TEMPO = 2,2,6,6-四甲基哌啶-N-氧基)作为助催化剂,并使用空气(O 2)作为氧化剂。它可以耐受各种官能化的苯甲醇和脂肪醇。
  • Rh(III)-Catalyzed Enaminone-Directed C–H Coupling with α-Diazo-α-phosphonoacetate for Reactivity Discovery: Fluoride-Mediated Dephosphonation for C–C Coupling Reactions
    作者:Chao Song、Chen Yang、Hua Zeng、Wenjing Zhang、Shan Guo、Jin Zhu
    DOI:10.1021/acs.orglett.8b01406
    日期:2018.7.6
    Rh(III)-catalyzed enaminone-directed C–H coupling with α-diazo-α-phosphonoacetate has been used for the identification of fluoride-mediated dephosphonation C–C coupling reactivity for the synthesis of 4-hydroxy-1-naphthoates. Intermolecular C–C coupling of α-phosphonoacetate and benzaldehyde for (E)-selective α,β-unsaturated ester synthesis has also been achieved.
    Rh(III)催化的与α-重氮-α-膦酰基乙酸酯结合的烯胺酮定向的C–H偶联已用于鉴定氟化物介导的膦酰基化的C–C偶联反应,用于合成4-羟基-1-萘甲酸酯。还实现了α-膦酰基乙酸酯和苯甲醛的分子间CC偶联,用于(E)-选择性α,β-不饱和酯的合成。
  • 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。
  • Hypervalent iodine(<scp>iii</scp>) induced oxidative olefination of benzylamines using Wittig reagents
    作者:Vijayalakshmi Ramavath、Bapurao D. Rupanawar、Satish G. More、Ajay H. Bansode、Gurunath Suryavanshi
    DOI:10.1039/d1nj01170g
    日期:——
    and secondary benzylamines using 2C-Wittig reagents, which provides easy access to α,β-unsaturated esters. Mild reaction conditions, good to excellent yields with high (E) selectivity, and a broad substrate scope are the key features of this reaction. We have successfully carried out the gram-scale synthesis of α,β-unsaturated esters.
    我们使用2C-Wittig试剂开发了高价碘(III)诱导的伯苄胺和仲苄胺的氧化烯化反应,该反应可轻松获得α,β-不饱和酯。温和的反应条件,具有高(E)选择性的良好至优异的产率以及广泛的底物范围是该反应的关键特征。我们已经成功地进行了克级的α,β-不饱和酯的合成。
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