2,2,2-tris(phenylthio)acetaldehyde | 96014-41-4

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 2,2,2-tris(phenylthio)acetaldehyde
• 英文别名: Tris(phenylsulfanyl)acetaldehyde；2,2,2-tris(phenylsulfanyl)acetaldehyde
• CAS: 96014-41-4
• 化学式: C₂₀H₁₆OS₃
• 分子量: 368.544
• InChiKey: KRONGMFVRYBCEI-UHFFFAOYSA-N

物化性质

• 沸点：
  464.4±45.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  93
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2,2,2-tris(phenylthio)acetaldehyde 在 吡啶 、 4-二甲氨基吡啶 、 正丁基锂 作用下， 反应 51.0h， 生成 1,1,1-tris(phenylthio)-2-acetoxy-3-<(trimethylsilyl)methyl>-3-butene
  参考文献：
  名称：

  Intramolecular palladium-catalyzed cycloadditions with a cleavable tether

  摘要：

  A facile synthesis of 2-(acyloxy)-3-methylene-4-(trimethylsilyl)butyric acids evolves from the use of tris(phenylthio)acetaldehyde as a practical glyoxylic ester equivalent. Introduction of the bifunctional donor of a [3 + 2] cycloaddition proceeds simply by esterification of an alcohol possessing TMM-PdL2 acceptor units. The synthetic flexibility of the sulfone leads to the choice of alpha, beta-unsaturated sulfones as the acceptors. Palladium-catalyzed cycloadditions proceed smoothly at temperatures as low as room temperature. Depending upon the substitution pattern and especially the conformation of the substrate, tethering the ester containing the bifunctional TMM unit at the carbon allylic to the acceptor provides substrates that predominantly to exclusively undergo cycloaddition rather than processes dominated by an alternative Pd(0)-catalyzed ionization. Since the ester linkage is easily cleaved, this sequence serves as a convenient strategy for controlled TMM-PdL2 cycloadditions. For example, the diastereofacial selectivity of this intramolecular process involves attack syn to the allylic oxygen in a six- or seven-membered-ring acceptor but anti to this oxygen in an intermolecular process. A diastereocontrolled cyclopentenone annulation is developed. Interestingly, the intramolecular cycloaddition of eight- and twelve-membered rings proceeds anti to the allylic oxygen. As an aside, the indefinite shelf life of the crystalline tris(phenylthio)acetaldehyde makes it a convenient glyoxylate synthon.

  DOI：

  10.1021/ja00019a037
• 作为产物：
  描述：

  2,2,2-tris(phenylthio)ethanol 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 生成 2,2,2-tris(phenylthio)acetaldehyde
  参考文献：
  名称：

  Intramolecular palladium-catalyzed cycloadditions with a cleavable tether

  摘要：

  A facile synthesis of 2-(acyloxy)-3-methylene-4-(trimethylsilyl)butyric acids evolves from the use of tris(phenylthio)acetaldehyde as a practical glyoxylic ester equivalent. Introduction of the bifunctional donor of a [3 + 2] cycloaddition proceeds simply by esterification of an alcohol possessing TMM-PdL2 acceptor units. The synthetic flexibility of the sulfone leads to the choice of alpha, beta-unsaturated sulfones as the acceptors. Palladium-catalyzed cycloadditions proceed smoothly at temperatures as low as room temperature. Depending upon the substitution pattern and especially the conformation of the substrate, tethering the ester containing the bifunctional TMM unit at the carbon allylic to the acceptor provides substrates that predominantly to exclusively undergo cycloaddition rather than processes dominated by an alternative Pd(0)-catalyzed ionization. Since the ester linkage is easily cleaved, this sequence serves as a convenient strategy for controlled TMM-PdL2 cycloadditions. For example, the diastereofacial selectivity of this intramolecular process involves attack syn to the allylic oxygen in a six- or seven-membered-ring acceptor but anti to this oxygen in an intermolecular process. A diastereocontrolled cyclopentenone annulation is developed. Interestingly, the intramolecular cycloaddition of eight- and twelve-membered rings proceeds anti to the allylic oxygen. As an aside, the indefinite shelf life of the crystalline tris(phenylthio)acetaldehyde makes it a convenient glyoxylate synthon.

  DOI：

  10.1021/ja00019a037

文献信息

• Intramolecular palladium-catalyzed cycloadditions with a cleavable tether
  作者：Barry M. Trost、Timothy A. Grese

  DOI：10.1021/ja00019a037

  日期：1991.9

  A facile synthesis of 2-(acyloxy)-3-methylene-4-(trimethylsilyl)butyric acids evolves from the use of tris(phenylthio)acetaldehyde as a practical glyoxylic ester equivalent. Introduction of the bifunctional donor of a [3 + 2] cycloaddition proceeds simply by esterification of an alcohol possessing TMM-PdL2 acceptor units. The synthetic flexibility of the sulfone leads to the choice of alpha, beta-unsaturated sulfones as the acceptors. Palladium-catalyzed cycloadditions proceed smoothly at temperatures as low as room temperature. Depending upon the substitution pattern and especially the conformation of the substrate, tethering the ester containing the bifunctional TMM unit at the carbon allylic to the acceptor provides substrates that predominantly to exclusively undergo cycloaddition rather than processes dominated by an alternative Pd(0)-catalyzed ionization. Since the ester linkage is easily cleaved, this sequence serves as a convenient strategy for controlled TMM-PdL2 cycloadditions. For example, the diastereofacial selectivity of this intramolecular process involves attack syn to the allylic oxygen in a six- or seven-membered-ring acceptor but anti to this oxygen in an intermolecular process. A diastereocontrolled cyclopentenone annulation is developed. Interestingly, the intramolecular cycloaddition of eight- and twelve-membered rings proceeds anti to the allylic oxygen. As an aside, the indefinite shelf life of the crystalline tris(phenylthio)acetaldehyde makes it a convenient glyoxylate synthon.