4-Methyl-4-phenyl-cyclohex-1-enecarboxylic acid 4-methyl-2-thioxo-thiazol-3-yl ester | 135616-25-0

• 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: 4-Methyl-4-phenyl-cyclohex-1-enecarboxylic acid 4-methyl-2-thioxo-thiazol-3-yl ester
• 英文别名: 4-Methyl-3-{[(4-methyl-4-phenyl-1-cyclohexen-1-YL)carbonyl]oxy}-1,3-thiazole-2(3H)-thione；(4-methyl-2-sulfanylidene-1,3-thiazol-3-yl) 4-methyl-4-phenylcyclohexene-1-carboxylate
• CAS: 135616-25-0
• 化学式: C₁₈H₁₉NO₂S₂
• 分子量: 345.486
• InChiKey: GIRJOERDXKYXPR-UHFFFAOYSA-N

物化性质

• 沸点：
  452.259±55.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.306±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  86.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-Methyl-4-phenyl-cyclohex-1-enecarboxylic acid 4-methyl-2-thioxo-thiazol-3-yl ester 在 偶氮二异丁腈 、 三氯溴甲烷 作用下， 以87%的产率得到(4-bromo-1-methyl-3-cyclohexen-1-yl)benzene
  参考文献：
  名称：

  Regioselective conversion of cycloalkanones to vinyl bromides with 1,2-functionality transposition. A general stratagem

  摘要：

  Cyclic beta-keto esters, available by regioselective acylation of cycloalkanone enolates, are rapidly transformed to alpha,beta-unsaturated acids. This functionality transposition allows the derived 3-hydroxy-4-methylthiazole-2-(3H)-thione derivatives to serve as precursors to synthetically useful vinyl bromides. The process involves heating the hydroxamate ester with AIBN in bromotrichloromethane solution. Alkylative and ring contractive variants of the methodology are highlighted. The short sequence makes available precursors to vinyl anions that are not otherwise conveniently accessible.

  DOI：

  10.1021/jo00021a044
• 作为产物：
  描述：

  3-羟基-4-甲基-2(3H)-噻唑硫酮 、 4-methyl-4-phenylcyclohexene-1-carboxylic acid 在 吡啶 、 4-二甲氨基吡啶 、 草酰氯 作用下， 生成 4-Methyl-4-phenyl-cyclohex-1-enecarboxylic acid 4-methyl-2-thioxo-thiazol-3-yl ester
  参考文献：
  名称：

  Regioselective conversion of cycloalkanones to vinyl bromides with 1,2-functionality transposition. A general stratagem

  摘要：

  Cyclic beta-keto esters, available by regioselective acylation of cycloalkanone enolates, are rapidly transformed to alpha,beta-unsaturated acids. This functionality transposition allows the derived 3-hydroxy-4-methylthiazole-2-(3H)-thione derivatives to serve as precursors to synthetically useful vinyl bromides. The process involves heating the hydroxamate ester with AIBN in bromotrichloromethane solution. Alkylative and ring contractive variants of the methodology are highlighted. The short sequence makes available precursors to vinyl anions that are not otherwise conveniently accessible.

  DOI：

  10.1021/jo00021a044

文献信息

• Regioselective conversion of cycloalkanones to vinyl bromides with 1,2-functionality transposition. A general stratagem
  作者：Leo A. Paquette、Karl Dahnke、Julien Doyon、Wei He、Kenetha Wyant、Dirk Friedrich

  DOI：10.1021/jo00021a044

  日期：1991.10

  Cyclic beta-keto esters, available by regioselective acylation of cycloalkanone enolates, are rapidly transformed to alpha,beta-unsaturated acids. This functionality transposition allows the derived 3-hydroxy-4-methylthiazole-2-(3H)-thione derivatives to serve as precursors to synthetically useful vinyl bromides. The process involves heating the hydroxamate ester with AIBN in bromotrichloromethane solution. Alkylative and ring contractive variants of the methodology are highlighted. The short sequence makes available precursors to vinyl anions that are not otherwise conveniently accessible.