3,5-Dimethyl-4-pyrrolidin-1-yl-5H-thiophen-2-one | 890933-71-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: 3,5-Dimethyl-4-pyrrolidin-1-yl-5H-thiophen-2-one
• 英文别名: 2,4-dimethyl-3-pyrrolidin-1-yl-2H-thiophen-5-one
• CAS: 890933-71-8
• 化学式: C₁₀H₁₅NOS
• 分子量: 197.301
• InChiKey: VITVZQLSWZNBFH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  45.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3,5-Dimethyl-4-pyrrolidin-1-yl-5H-thiophen-2-one 在 戴斯-马丁氧化剂 、 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 2.5h， 生成 2,4-Dimethyl-5-oxo-3-pyrrolidin-1-yl-2,5-dihydro-thiophene-2-carbaldehyde
  参考文献：
  名称：

  Novel route to 5-position vinyl derivatives of thiolactomycin: olefination versus deformylation

  摘要：

  Vinyl and diene derivatives of thiolactomycin have been prepared via Horner-Wadsworth-Emmons olefination from protected 5-formyl-3,5-dimethylthiotetronic acid. Several 4-position protecting groups and a variety of phosphonates were evaluated, with MOM protection and beta-ketophosphonates yielding the highest ratio of the desired product to deformylated product. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.03.058
• 作为产物：
  描述：

  在 戴斯-马丁氧化剂 、 N,N-二异丙基乙胺 、 lithium chloride 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 1.0h， 生成 3,5-Dimethyl-4-pyrrolidin-1-yl-5H-thiophen-2-one
  参考文献：
  名称：

  Novel route to 5-position vinyl derivatives of thiolactomycin: olefination versus deformylation

  摘要：

  Vinyl and diene derivatives of thiolactomycin have been prepared via Horner-Wadsworth-Emmons olefination from protected 5-formyl-3,5-dimethylthiotetronic acid. Several 4-position protecting groups and a variety of phosphonates were evaluated, with MOM protection and beta-ketophosphonates yielding the highest ratio of the desired product to deformylated product. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.03.058