(E)-3-oxo-5-phenyl-1-(2-thienyl)-4-penten-1-yne | 905946-23-8

• 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: (E)-3-oxo-5-phenyl-1-(2-thienyl)-4-penten-1-yne
• 英文别名: (e)-3-Oxo-5-phenyl-1-(2-thienyl)-4-penten-1-yne；(E)-1-phenyl-5-thiophen-2-ylpent-1-en-4-yn-3-one
• CAS: 905946-23-8
• 化学式: C₁₅H₁₀OS
• 分子量: 238.31
• InChiKey: BRQUMBUCYZNXHV-CMDGGOBGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  45.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (E)-3-oxo-5-phenyl-1-(2-thienyl)-4-penten-1-yne 在 sodium hydrogensulfide 作用下， 以 乙二醇甲醚 为溶剂， 以81%的产率得到2,3-dihydro-2-phenyl-6-(2-thienyl)thiopyran-4-one
  参考文献：
  名称：

  Synthesis of unsymmetrically 2,6-disubstituted 2,3-dihydrothiopyran-4-ones

  摘要：

  A series of 2,3-dihydrothiopyran-4-one derivatives with unequal substituents in the 2- and 6-position have been prepared by double conjugate addition of sulfide to enynones. These starting materials were accessed in two steps from terminal alkynes and alpha,beta-unsaturated aldehydes. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.05.080
• 作为产物：
  描述：

  (E)-3-hydroxy-5-phenyl-1-(2-thienyl)-4-penten-1-yne 在 manganese(IV) oxide 作用下， 以 二氯甲烷 为溶剂， 以99%的产率得到(E)-3-oxo-5-phenyl-1-(2-thienyl)-4-penten-1-yne
  参考文献：
  名称：

  Synthesis of unsymmetrically 2,6-disubstituted 2,3-dihydrothiopyran-4-ones

  摘要：

  A series of 2,3-dihydrothiopyran-4-one derivatives with unequal substituents in the 2- and 6-position have been prepared by double conjugate addition of sulfide to enynones. These starting materials were accessed in two steps from terminal alkynes and alpha,beta-unsaturated aldehydes. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.05.080

文献信息

• Synthesis of 2,3-Dihydrothiopyran-4-ones from 3-Oxo-1-pentene-4-ynes
  作者：Anna Rosiak、Ralf M. Müller、Jens Christoffers

  DOI：10.1007/s00706-006-0571-4

  日期：2007.1

  3-Oxo-1-pentene-4-ynes were converted with sodium sulfide or hydrogensulfide to give 2,6-disubstituted 2,3-dihydrothiopyran-4-one derivatives. The starting materials were prepared in two steps from terminal alkynes and alpha,beta-unsaturated aldehydes.