(1R,2S)-methyl 2-(1-hydroxy-3-methylbutyl)oxirane-2-carboxylate

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羟基酸及其衍生物
• 英文名称: (1R,2S)-methyl 2-(1-hydroxy-3-methylbutyl)oxirane-2-carboxylate
• 英文别名: methyl (2S)-2-[(1R)-1-hydroxy-3-methylbutyl]oxirane-2-carboxylate
• 化学式: C₉H₁₆O₄
• 分子量: 188.224
• InChiKey: BDYVSIFQEBIWHD-APPZFPTMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  59.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  三光气 、 (1R,2S)-methyl 2-(1-hydroxy-3-methylbutyl)oxirane-2-carboxylate 、 苯硫酚 在 sodium hydride 、 吡啶 作用下， 以 四氢呋喃 、 mineral oil 为溶剂， 反应 15.25h， 以76%的产率得到(4S,5R)-methyl 5-isobutyl-2-oxo-4-((phenylthio)methyl)-1,3-dioxolane-4-carboxylate
  参考文献：
  名称：

  Study of the stereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters

  摘要：

  The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita-Baylis-Hillman reaction. The resulting epoxyesters were treated with thiophenol for transformation into 2,3-dihydroxy-2-((phenylthio)methyl), which upon treatment with triphosgene afforded the corresponding cyclic carbonates. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.11.014
• 作为产物：
  描述：

  异戊醛 在 三乙烯二胺 、 叔丁基过氧化氢 、 甲基锂 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 正己烷 、 水 、 甲苯 为溶剂， 反应 48.0h， 生成 (1R,2S)-methyl 2-(1-hydroxy-3-methylbutyl)oxirane-2-carboxylate
  参考文献：
  名称：

  Study of the stereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters

  摘要：

  The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita-Baylis-Hillman reaction. The resulting epoxyesters were treated with thiophenol for transformation into 2,3-dihydroxy-2-((phenylthio)methyl), which upon treatment with triphosgene afforded the corresponding cyclic carbonates. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.11.014

文献信息

• Study of the stereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters
  作者：Antonio Latorre、José A. Sáez、Santiago Rodríguez、Florenci V. González

  DOI：10.1016/j.tet.2013.11.014

  日期：2014.1

  The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita-Baylis-Hillman reaction. The resulting epoxyesters were treated with thiophenol for transformation into 2,3-dihydroxy-2-((phenylthio)methyl), which upon treatment with triphosgene afforded the corresponding cyclic carbonates. (C) 2013 Elsevier Ltd. All rights reserved.