(S)-3-(2-allylphenoxy)propane-1,2-diol | 476169-18-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (S)-3-(2-allylphenoxy)propane-1,2-diol
• 英文别名: (s)-3-(2-Allylphenoxy)-propane-1,2,-diol；(2S)-3-(2-prop-2-enylphenoxy)propane-1,2-diol
• CAS: 476169-18-3
• 化学式: C₁₂H₁₆O₃
• 分子量: 208.257
• InChiKey: NRIXNDFJJSOBCR-NSHDSACASA-N

物化性质

• 熔点：
  47-49 °C
• 沸点：
  363.4±32.0 °C(Predicted)
• 密度：
  1.118±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  49.7
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-3-(2-allylphenoxy)propane-1,2-diol 在 氯化亚砜 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以100%的产率得到(4R)-4-(2-allylphenoxymethyl)-1,3,2-dioxathiolane 2-oxide
  参考文献：
  名称：

  环亚硫酸盐，由缩水甘油合成1-烷基氨基-3-芳氧基-2-丙醇的关键中间体

  摘要：

  A number of 3-aryloxypropanedioles were obtained by treating glycidol with phenols. The latter with thionyl chloride afforded 4-aryloxymethyl-1,3,2-dioxathiolane 2-oxides. These compounds were also obtained from 4-chloromethyl-1,3,2-dioxathiolane 2-oxides by substitution aryloxy group for chlorine. The cyclic sulfides synthesized are universal intermediates in the synthesis of chiral aryloxypropanolamines among which are known beta-adrenoblockaders, cardiovascular drugs. From (S)-glycidol, (S)-alprenolol, (S)-propanolol, and (S)-thymolol were synthesized.

  DOI：

  10.1023/a:1015561532507
• 作为产物：
  描述：

  (S)-3-氯-1,2-丙二醇 、 2-烯丙基酚 在 sodium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 反应 3.5h， 以70%的产率得到(S)-3-(2-allylphenoxy)propane-1,2-diol
  参考文献：
  名称：

  一系列均匀取代的苯基甘油醚中的三种不同类型的手性驱动结晶。

  摘要：

  七个手性芳基甘油醚2-RC（6）H（4）-O-CH（2）CH（OH）CH（2）OH（R ​​= H，Me，Et，烯丙基，n-Pr，i-Pr，叔-Bu）以外消旋和垢的形式合成。测量了每个物种的外消旋和尺度样品的红外光谱，熔点和熔融焓，导出了液态混合的对映异构体的熵和外消旋化合物形成的Gibbs自由能，并重建了二元相图。整个家族。对这四种物质的固态外消旋化合物稳定性进行了排名。建立了注册手性药物美芬素及其乙基类似物的自发拆分。在叔丁基衍生物的溶液结晶过程中，形成了亚稳态异常聚集体，形成了在晶胞中具有三个独立的R *和一个独立的S *分子的晶体。

  DOI：

  10.1002/chir.20648

文献信息

• Jacobsen-type enantioselective hydrolysis of aryl glycidyl ethers.³¹P NMR analysis of the enantiomeric composition of oxiranes
  作者：A. A. Bredikhin、E. I. Strunskaya、V. G. Novikova、N. M. Azancheev、D. R. Sharafutdinova、Z. A. Bredikhina

  DOI：10.1023/b:rucb.0000024851.29744.21

  日期：2004.1

  The enantioselective partial hydrolysis of a number of racemic aryl glycidyl ethers in the presence of chiral Co(salen)-catalyst was studied. The enantiomeric composition of the isolated (R)-aryl glycidyl ethers was analyzed by 31P NMR using optically active substituted 2-chloro-1,3,2-dioxaphospholanes. A synthesis of β-adrenoblocking agents (S)-toliprolol and (S)-moprolol based on the simultaneously

  研究了在手性 Co(salen) 催化剂存在下，许多外消旋芳基缩水甘油醚的对映选择性部分水解。分离的(R)-芳基缩水甘油醚的对映体组成通过31P NMR使用光学活性取代的2-氯-1,3,2-二氧杂环戊烷进行分析。提出了基于同时获得的 (S)-3-芳氧基丙烷-1,2-二醇合成 β-肾上腺素阻滞剂 (S)-toliprolol 和 (S)-moprolol。
• Systematic search for conglomerates among glycerol aromatic monoethers: guaifenesin and mephenesin are the cases
  作者：Alexander A. Bredikhin、Zemfira A. Bredikhina、Sergey N. Lazarev、Dmitry V. Savel’ev

  DOI：10.1070/mc2003v013n03abeh001752

  日期：2003.1

  Within the family of biologically active 3-aryloxy-1,2-propanediols, three new conglomerate-forming compounds have been found resolved into enantiomers using the entrainment procedure.
• ——
  作者：Z. A. Bredikhina、D. V. Savel'ev、A. A. Bredikhin

  DOI：10.1023/a:1015561532507

  日期：——

  A number of 3-aryloxypropanedioles were obtained by treating glycidol with phenols. The latter with thionyl chloride afforded 4-aryloxymethyl-1,3,2-dioxathiolane 2-oxides. These compounds were also obtained from 4-chloromethyl-1,3,2-dioxathiolane 2-oxides by substitution aryloxy group for chlorine. The cyclic sulfides synthesized are universal intermediates in the synthesis of chiral aryloxypropanolamines among which are known beta-adrenoblockaders, cardiovascular drugs. From (S)-glycidol, (S)-alprenolol, (S)-propanolol, and (S)-thymolol were synthesized.
• Three different types of chirality-driven crystallization within the series of uniformly substituted phenyl glycerol ethers
  作者：Alexander A. Bredikhin、Zemfira A. Bredikhina、Victorina G. Novikova、Alexander V. Pashagin、Dmitry V. Zakharychev、Aidar T. Gubaidullin

  DOI：10.1002/chir.20648

  日期：2008.10

  derived and binary phase diagrams were reconstructed for the whole family. Solid racemic compounds stabilities were ranked for the four substances. Spontaneous resolution was established for the registered chiral drug mephenesin and its ethyl analogue. Metastable anomalous conglomerate, forming crystals having three independent R* and one independent S* molecules in the unit cell, is formed during solution

  七个手性芳基甘油醚2-RC（6）H（4）-O-CH（2）CH（OH）CH（2）OH（R ​​= H，Me，Et，烯丙基，n-Pr，i-Pr，叔-Bu）以外消旋和垢的形式合成。测量了每个物种的外消旋和尺度样品的红外光谱，熔点和熔融焓，导出了液态混合的对映异构体的熵和外消旋化合物形成的Gibbs自由能，并重建了二元相图。整个家族。对这四种物质的固态外消旋化合物稳定性进行了排名。建立了注册手性药物美芬素及其乙基类似物的自发拆分。在叔丁基衍生物的溶液结晶过程中，形成了亚稳态异常聚集体，形成了在晶胞中具有三个独立的R *和一个独立的S *分子的晶体。