methyl 3-(N-4-methoxyphenyl)amino-2-methyl-4,4,4-trifluoro-2-butenoate | 249939-32-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: methyl 3-(N-4-methoxyphenyl)amino-2-methyl-4,4,4-trifluoro-2-butenoate
• 英文别名: methyl (Z)-4,4,4-trifluoro-3-(4-methoxyanilino)-2-methyl-2-butenoate；methyl 4,4,4-trifluoro-3-(4-methoxyanilino)-2-methyl-2-butenoate；methyl (Z)-4,4,4-trifluoro-3-(4-methoxyanilino)-2-methylbut-2-enoate
• CAS: 249939-32-0
• 化学式: C₁₃H₁₄F₃NO₃
• 分子量: 289.254
• InChiKey: DOGRCJPCNDLZQU-FLIBITNWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  47.6
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  methyl 3-(N-4-methoxyphenyl)amino-2-methyl-4,4,4-trifluoro-2-butenoate 在 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 zinc(II) iodide 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 26.0h， 生成 (2R*,3R*)-4,4,4-trifluoro-3-(4-methoxyanilino)-2-methylbutan-1-ol
  参考文献：
  名称：

  First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters

  摘要：

  [GRAPHICS]A new two-step approach for the diastereoselective synthesis of the syn alpha-methyl beta-fluoroalkyl beta-amino esters 4 has been developed. This approach is based on the chemical reduction of the fluorinated beta-enamino esters 3, which have been previously obtained from imidoyl chlorides 1 and lithium ester enolates, with Znl(2)/NaBH4 as the reducing agent. The process takes place with high syn diastereoselectivity and good to excellent yields. A metal-chelated six-membered model has been suggested to explain the stereochemical outcome of the reduction reaction.

  DOI：

  10.1021/ol990774o
• 作为产物：
  描述：

  methyl S-(1-((N-4-methoxyphenyl)imino)-2,2,2-trifluoroethyl)thiolactate 在 lithium diisopropyl amide 作用下， 以 四氢呋喃 为溶剂， 反应 9.0h， 生成 methyl 3-(N-4-methoxyphenyl)amino-2-methyl-4,4,4-trifluoro-2-butenoate
  参考文献：
  名称：

  A Trial toward the Synthesis of γ-Fluorinated β-Amino-α-thiohydroxyamino Acid:  A Finding of Desulfurizative C−C Bond Formation in Thio-Wittig-Type Rearrangement of S-(N-Aryltrifluoroacetimidoyl)thioglycolates

  摘要：

  DOI：

  10.1021/jo0010330

文献信息

• First Highly Diastereoselective Synthesis of <i>s</i><i>yn</i> α-Methyl β-Fluoroalkyl β-Amino Esters
  作者：Santos Fustero、Belén Pina、Marta García de la Torre、Antonio Navarro、Carmen Ramírez de Arellano、Antonio Simón

  DOI：10.1021/ol990774o

  日期：1999.10.1

  [GRAPHICS]A new two-step approach for the diastereoselective synthesis of the syn alpha-methyl beta-fluoroalkyl beta-amino esters 4 has been developed. This approach is based on the chemical reduction of the fluorinated beta-enamino esters 3, which have been previously obtained from imidoyl chlorides 1 and lithium ester enolates, with Znl(2)/NaBH4 as the reducing agent. The process takes place with high syn diastereoselectivity and good to excellent yields. A metal-chelated six-membered model has been suggested to explain the stereochemical outcome of the reduction reaction.
• New Strategy for the Stereoselective Synthesis of Fluorinated β-Amino Acids
  作者：Santos Fustero、Belén Pina、Esther Salavert、Antonio Navarro、M. Carmen Ramírez de Arellano、Antonio Simón Fuentes

  DOI：10.1021/jo025621k

  日期：2002.7.1

  Racemic and chiral nonracemic alpha-substituted and alpha-unsubstituted beta-fluoroalkyl beta-amino acid derivatives 6 and 9 have been synthesized in two steps starting from fluorinated imidoyl chlorides 1 and ester enolates. This approach is based on the chemical reduction of previously obtained gamma-fluorinated beta-enamino esters 4 by using ZnI2/NaBH4 in a nonchelated aprotic medium (dry CH2Cl2) as the reducing agent. A metal-chelated six-membered model has been suggested to explain the stereochemical outcome of the reduction reaction. The process takes place with high yields and with moderate to good diastereoselectivity. The best results related to diastereoselective reduction of chiral beta-enamino esters 4 were provided by the use of (-)-8-phenylmenthol as a chiral auxiliary.
• A Trial toward the Synthesis of γ-Fluorinated β-Amino-α-thiohydroxyamino Acid:  A Finding of Desulfurizative C−C Bond Formation in Thio-Wittig-Type Rearrangement of <i>S</i>-(<i>N</i>-Aryltrifluoroacetimidoyl)thioglycolates
  作者：Kenji Uneyama、Hironari Ohkura、Jian Hao、Hideki Amii

  DOI：10.1021/jo0010330

  日期：2001.2.1