Methyl 2-(p-Methoxyphenyl)-6-methoxy-5-cyano-3,4-dihydro-2H-pyran-4-carboxylate | 77321-38-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: Methyl 2-(p-Methoxyphenyl)-6-methoxy-5-cyano-3,4-dihydro-2H-pyran-4-carboxylate
• 英文别名: methyl 5-cyano-6-methoxy-2-(4-methoxyphenyl)-3,4-dihydro-2H-pyran-4-carboxylate
• CAS: 77321-38-1
• 化学式: C₁₆H₁₇NO₅
• 分子量: 303.315
• InChiKey: UGPLDNZZGPYHDQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  77.8
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  4-甲氧基苯乙烯 、 dimethyl cyanofumarate 在 1,1-二苯-2-苦基肼 作用下， 以 氘代乙腈 为溶剂， 反应 118.0h， 以33.7%的产率得到Methyl 2-(p-Methoxyphenyl)-6-methoxy-5-cyano-3,4-dihydro-2H-pyran-4-carboxylate
  参考文献：
  名称：

  Trapping tetramethylene biradical intermediates in cycloaddition reactions of p-methoxystyrene by vinyl copolymerization reactions

  摘要：

  DOI：

  10.1021/jo00327a022

文献信息

• 6-alkoxy-3,4-dihydro-2h-pyrans from substituted α,β-unsaturated esters
  作者：H.K. Hall、H.A.A. Rasoul、M. Gillard、M. Abdelkader、P. Nogues、R.C. Sentman

  DOI：10.1016/s0040-4039(00)86901-4

  日期：1982.1

  Cycloaddition reactions of substituted α,β-unsaturated esters with various electronich olefins lead to 6-alkoxy-3,4-dihydro-2H-pyrans.

  取代的α，β-不饱和酯与各种电子烯烃的环加成反应会生成6-烷氧基-3,4-二氢-2H-吡喃。
• Influence of Lewis Acids on the Cycloaddition Reactions of Cyano- and Carbomethoxy-Substituted Olefins
  作者：Warunee Srisiri、Anne Buyle Padias、H. K. Hall

  DOI：10.1021/jo00097a054

  日期：1994.9

  The reactions of electrophilic olefins substituted with cyano and/or carbomethoxy groups with donor olefins are investigated. The donor olefins include, in order of decreasing donor character, phenyl vinyl sulfide, isobutyl vinyl ether, tert-butyldimethylsilyl vinyl ether, p-methoxy- and p-methylstyrene, and styrene. The reactions vary ii om [2 + 2] cycloadditions to Diels-Alder reactions to spontaneous free radical copolymerizations. The course of the reaction is determined by both the electron disparity between the two reacting olefins and by the substitution pattern on the electrophilic olefin. Lewis acids (ZnCl2 or ethereal LiClO4) are added to form complexes with the acceptor olefins, resulting in a larger electron disparity between the reactants. With the highly electrophilic olefins with gem-dicyano groups, such as tetracyanoethylene, dimethyl 1,1-dicyanoethylene-2,2-dicarboxylate, and methyl beta,beta-dicyanoacrylate, [2 + 2] cycloadditions occur at room temperature, except for the reaction of TCNE with styrene which has to be carried out in 5 M ethereal LiClO4. With olefins containing one cyano and one carbomethoxy group on the same carbon, dimethyl dicyanofumarate and dimethyl cyanofumarate, inverse electron demand Diels-Alder cycloaddition involving the ester substituent dominates in reactions with the most nucleophilic olefins. The [2 + 2] cycloadducts can be obtained in the presence of Lewis acid. With olefins with two carbomethoxy-substituents on the same carbon, dimethyl 2-cyanoethene-1,1-dicarboxylate and trimethyl ethylenetricarboxylate, the reactions are much slower, and [2 + 4] cycloaddition dominates with the most reactive donor olefins, while the [2 + 2] cycloadduct can be obtained in the presence of Lewis acid. With several acceptor olefins, free radical copolymerizations compete with the cycloadditions when reacted with the least reactive donor olefins. The reaction tendencies are discussed in light of the electron disparity between the olefins. The influence of the Lewis acid on the conformational equilibria and on the reaction course is also addressed.
• HALL, H. K. ,, JR;RASOUL, H. A. A.;GILLARD, M.;ABDELKADER, M.;NOGUES, P.;+, TETRAHEDRON LETT., 1982, 23, N 6, 603-606
  作者：HALL, H. K. ,, JR、RASOUL, H. A. A.、GILLARD, M.、ABDELKADER, M.、NOGUES, P.、+

  DOI：——

  日期：——