Ethyl α-(2-formylphenyl)acrylate | 152303-03-2

• 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 α-(2-formylphenyl)acrylate
• 英文别名: ethyl 2-(2-formylphenyl)acrylate；Ethyl 2-(2-formylphenyl)prop-2-enoate
• CAS: 152303-03-2
• 化学式: C₁₂H₁₂O₃
• 分子量: 204.225
• InChiKey: BXSHNAHUESDOKJ-UHFFFAOYSA-N

物化性质

• 沸点：
  345.1±35.0 °C(Predicted)
• 密度：
  1.113±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Ethyl α-(2-formylphenyl)acrylate 在 盐酸羟胺 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 18.0h， 生成
  参考文献：
  名称：

  Copper(I) salt-mediated arylation of phosphinyl-stabilized carbanions and synthetic application to heterocyclic compounds

  摘要：

  The copper-mediated reaction of phosphinyl-stabilized carbanions 2a-c with aryl halides 1a-i in DMF or HMPA produced (arylmethyl)phosphonates 3-11 in good yields. Similar treatment of N-(2-iodophenyl)- and N-(2-iodophenyl)-N-methyl-alpha-(diethoxyphosphinyl)acetamides (12 and 14) led to 2-[(diethoxyphosphinyl)methyl]benzoxazole (13) and 1-methyl-3-(diethoxyphosphinyl)oxindole (15) in 71 and 85% yields, respectively. 4-(Ethoxycarbonyl)-3,4-dihydroisoquinoline N-oxide (33) was synthesized by the reaction of ethyl alpha-(o-formylphenyl)acrylate (31), derived from 6 and paraformaldehyde,with hydroxylamine. The cycloaddition of 33 to olefins such as dimethyl maleate, methyl acrylate, and styrene was studied.

  DOI：

  10.1021/jo00077a018
• 作为产物：
  描述：

  2-溴苯甲醛乙烯醛 在 正丁基锂 、 碘 、 sodium hexamethyldisilazane 作用下， 以 四氢呋喃 、 正己烷 、 丙酮 、 甲苯 为溶剂， 反应 21.75h， 生成 Ethyl α-(2-formylphenyl)acrylate
  参考文献：
  名称：

  二苯萘衍生物氟化苯并双环均烯丙基胺的不对称烯丙基化/ RCM介导合成

  摘要：

  通过不对称烯丙基化/闭环复分解（RCM）序列合成了对映体富集的氟化苯并稠合双环均烯丙基胺。该序列是使用α-三氟甲基苯乙烯衍生物作为关键中间体，通过微波辐射合成的。通过比较研究已经揭示了这种取代基所产生的极大的失活效果。

  DOI：

  10.1021/acs.joc.6b01590

文献信息

• Enantioselective N‐Heterocyclic Carbene Catalyzed Cyclopentene Synthesis via the β‐Azolium Ylide
  作者：Lydia Scott、Yuji Nakano、Changhe Zhang、David W. Lupton

  DOI：10.1002/anie.201804271

  日期：2018.8.6

  cycloisomerization of electron‐poor 1,5‐dienes via the β‐azolium ylide to give enantioenriched cyclopentenes. The reaction is mediated by a chiral N‐heterocyclic carbene (NHC) catalyst, exploits readily available substrates, has good generality (17 examples), and displays excellent enantioselectivity (mostly >94:6). Studies demonstrating the viability of a related dynamic kinetic resolution are reported, as

  在这里，我们报道了贫电子的1,5-二烯通过β-偶氮鎓内酯的环异构化反应，得到对映体富集的环戊烯。该反应由手性N-杂环卡宾（NHC）催化剂介导，利用容易获得的底物，具有良好的通用性（17个实例），并且显示出出色的对映选择性（大多数> 94：6）。报道了证明相关动态动力学分辨率的可行性的研究，以及具有替代系链和衍生化的研究。
• Hydroacylation of 2-Vinyl Benzaldehyde Systems:  An Efficient Method for the Synthesis of Chiral 3-Substituted Indanones
  作者：Kousik Kundu、James V. McCullagh、Andrew T. Morehead

  DOI：10.1021/ja0564416

  日期：2005.11.23

  Asymmetric rhodium-catalyzed hydroacylation has been utilized in the synthesis of 3-substituted indanones with high conversions and enantioselectivity. The hydroacylation reaction of 2-vinyl benzaldehyde had been previously reported to give a low yield of indanone and an unidentified product. We have identified this compound as a dimer of the starting material. Substitution at the alpha-position of

  不对称铑催化加氢酰化已用于合成具有高转化率和对映选择性的 3-取代茚满酮。之前曾报道过 2-乙烯基苯甲醛的加氢酰化反应会产生低产率的茚满酮和未鉴定的产物。我们已将此化合物鉴定为起始材料的二聚体。在 2-乙烯基苯甲醛底物的 α 位取代可阻止竞争性二聚反应，并使反应以通常大于 90% 的产率进行。在大多数情况下，使用 BINAP 作为手性配体可获得良好的化学产率和大于 95% 的对映选择性。
• Minami Toru, Isonaka Takeshi, Okada Yoshiharu, Ichikawa Junji, J. Org. Chem, 58 (1993) N 25, S 7009-7015
  作者：Minami Toru, Isonaka Takeshi, Okada Yoshiharu, Ichikawa Junji

  DOI：——

  日期：——
• Asymmetric Allylation/RCM-Mediated Synthesis of Fluorinated Benzo-Fused Bicyclic Homoallylic Amines As Dihydronaphthalene Derivatives
  作者：Daniel M. Sedgwick、Pablo Barrio、Antonio Simón、Raquel Román、Santos Fustero

  DOI：10.1021/acs.joc.6b01590

  日期：2016.10.7

  Enantiomerically enriched fluorinated benzo-fused bicyclic homoallylic amines have been synthesized through an asymmetric allylation/ring closing metathesis (RCM) sequence. This sequence has been carried out using α-trifluoromethylstyrene derivatives as key intermediates, synthesized by microwave radiation. The great deactivating effect exerted by such substituents has been brought to light by a comparative

  通过不对称烯丙基化/闭环复分解（RCM）序列合成了对映体富集的氟化苯并稠合双环均烯丙基胺。该序列是使用α-三氟甲基苯乙烯衍生物作为关键中间体，通过微波辐射合成的。通过比较研究已经揭示了这种取代基所产生的极大的失活效果。
• Copper(I) salt-mediated arylation of phosphinyl-stabilized carbanions and synthetic application to heterocyclic compounds
  作者：Toru Minami、Takeshi Isonaka、Yoshiharu Okada、Junji Ichikawa

  DOI：10.1021/jo00077a018

  日期：1993.12

  The copper-mediated reaction of phosphinyl-stabilized carbanions 2a-c with aryl halides 1a-i in DMF or HMPA produced (arylmethyl)phosphonates 3-11 in good yields. Similar treatment of N-(2-iodophenyl)- and N-(2-iodophenyl)-N-methyl-alpha-(diethoxyphosphinyl)acetamides (12 and 14) led to 2-[(diethoxyphosphinyl)methyl]benzoxazole (13) and 1-methyl-3-(diethoxyphosphinyl)oxindole (15) in 71 and 85% yields, respectively. 4-(Ethoxycarbonyl)-3,4-dihydroisoquinoline N-oxide (33) was synthesized by the reaction of ethyl alpha-(o-formylphenyl)acrylate (31), derived from 6 and paraformaldehyde,with hydroxylamine. The cycloaddition of 33 to olefins such as dimethyl maleate, methyl acrylate, and styrene was studied.