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3-(4-benzyloxyphenyl)-2-cyano-acrylic acid ethyl ester | 116592-71-3

中文名称
——
中文别名
——
英文名称
3-(4-benzyloxyphenyl)-2-cyano-acrylic acid ethyl ester
英文别名
3-(4-benzyloxy-phenyl)-2-cyano-ethyl acrylate;ethyl 3-(4-benzyloxyphenyl)-2-cyanoacrylate;Ethyl 2-cyano-3-(4-phenylmethoxyphenyl)prop-2-enoate
3-(4-benzyloxyphenyl)-2-cyano-acrylic acid ethyl ester化学式
CAS
116592-71-3
化学式
C19H17NO3
mdl
MFCD03939602
分子量
307.349
InChiKey
XFCLUVIWRQQLPP-UHFFFAOYSA-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):
    3.9
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.157
  • 拓扑面积:
    59.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • 一种3-(4-苄氧基苯基)-2-氰基丙烯酸乙酯的合成工艺
    申请人:上海应用技术大学
    公开号:CN108456151A
    公开(公告)日:2018-08-28
    本发明公开了一种3‑(4‑苄氧基苯基)‑2‑氰基丙烯酸乙酯的合成工艺。本发明的合成工艺具体如下:1)惰性气氛下,将对羟基苯甲醛、苄卤和碱、溶剂和催化剂常温混合搅拌3‑10小时,之后倒入水中,用萃取剂进行萃取,再依次将有机相水洗、干燥和浓缩得到中间体4‑(苯基甲氧基)苯甲醛;(2)惰性气氛下,将4‑(苯基甲氧基)苯甲醛、乙酸、氰基乙酸乙酯和催化量的哌啶在甲苯中回流反应3‑12小时;反应结束后,冷却至室温,加入淬灭剂,有机相依次经水洗、干燥、浓缩和纯化得到3‑(4‑苄氧基苯基)‑2‑氰基丙烯酸乙酯。本发明生成成本低、收率高,后处理简单。
  • The preparation and reaction of enolates within micro reactors
    作者:Charlotte Wiles、Paul Watts、Stephen J. Haswell、Esteban Pombo-Villar
    DOI:10.1016/j.tet.2005.08.076
    日期:2005.11
    Over the past 5 years, interest in the miniaturisation of chemical synthesis has grown rapidly, however in order to facilitate transfer of the technology from its current position as a research tool to industrial applications, a core understanding of the challenges associated with transferring reactions from the macro to the micro domain is required. This paper therefore aims to broach this problem by investigating the application of micro reactors to a range of commonly employed synthetic reactions including acylation, aldol, alkylation, 1,4-conjugate addition (Michael addition) and the Knoevenagel condensation. Comparison of the results obtained with traditional batch techniques enable us to highlight some of the advantages associated with micro reaction technology. (c) 2005 Elsevier Ltd. All rights reserved.
  • Synthesis and Biological Activity of Novel Acridinylidene and Benzylidene thiazolidinediones
    作者:R.H. Mourão、T.G. Silva、A.L.M. Soares、E.S. Vieira、J.N. Santos、M.C.A. Lima、V.L.M. Lima、S.L. Galdino、J. Barbe、I.R. Pitta
    DOI:10.1016/j.ejmech.2005.06.002
    日期:2005.11
    A novel set of acridinylidene thiazolidinediones and benzylidene thiazolidinediones was synthesized by nucleophilic addition of cyanoacrylates. Some of these compounds were evaluated for their glucose lowering capability and their effects on the triglyceride level in alloxan diabetic mice. (c) 2005 Elsevier SAS. All rights reserved.
  • Solid-Supported Continuous Flow Synthesis in Microreactors Using Electroosmotic Flow
    作者:Nikzad Nikbin、Paul Watts
    DOI:10.1021/op049857x
    日期:2004.11.1
    This paper reports the fabrication of a microreactor suitable for use with supported reagents. We demonstrate that the electroosmotic flow can be used to move the reagents over a solid-supported catalyst bed. It is demonstrated that it is important that the support should not swell in organic solvents to obtain reproducible flow, and it is shown that silica supports fulfill this criteria. Silica-functionalised piperazine is used in a variety of Knoevenagel reactions to give the product in high conversion.
  • Brandao; Andrade; Pereira, Heterocyclic Communications, 2004, vol. 10, # 1, p. 9 - 14
    作者:Brandao、Andrade、Pereira、Barbosa Filho、Lima、Galdino、Pitta、Barbe
    DOI:——
    日期:——
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