rac-3-(2-tert-butylphenoxy)propane-1,2-diol | 55143-03-8

• 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: rac-3-(2-tert-butylphenoxy)propane-1,2-diol
• 英文别名: 3-(2-tert-butylphenoxy)propane-1,2-diol
• CAS: 55143-03-8
• 化学式: C₁₃H₂₀O₃
• 分子量: 224.3
• InChiKey: QIXYTBXFUXHZCR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.54
• 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：

  乙酸乙烯酯 、 rac-3-(2-tert-butylphenoxy)propane-1,2-diol 在 三乙胺 作用下， 以 乙醚 为溶剂， 反应 100.0h， 生成 [3-(2-tert-butylphenoxy)-2-hydroxypropyl] acetate 、 、 [(2S)-2-acetyloxy-3-(2-tert-butylphenoxy)propyl] acetate
  参考文献：
  名称：

  Kinetic resolution of acyclic 1,2-diols using a sequential lipase-catalyzed transesterification in organic solvents

  摘要：

  A method for the kinetic resolution of 3-(aryloxy)-1,2-propanediols rac-1a-n without additional protection-deprotection steps using a lipase-catalyzed sequential transesterification with lipase amnno PS has been developed. In the first step of this one-pot procedure the racemic 1,2-diols are acylated regioselectively at the primary hydroxy group without enantioselection. The subsequent acylation at the secondary hydroxy group of the formed primary monoacetate is responsible for high enantioselection. The enantioselectivity of this transformation depends significantly on the substitution pattern of the aryl ring and the organic solvent used. 3-(Aryloxy)-1,2-propanediols with substituents in the para-position show a much higher enantioselectivity than the corresponding derivatives with ortho-substituents. Among other substrates, the pharmaceuticals Mephenesin, Guaifenesin, and Chlorphenesin have been resolved. The replacement of the aryloxy by alkyl substituent causes a dramatic decrease of enantioselectivity.

  DOI：

  10.1021/jo00081a018
• 作为产物：
  描述：

  2-叔丁基苯酚 、 3-氯-1,2-丙二醇 在 sodium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 反应 3.5h， 以63%的产率得到rac-3-(2-tert-butylphenoxy)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

• Auzou; Rips; Derappe, European Journal of Medicinal Chemistry, 1974, vol. 9, # 5, p. 548 - 554
  作者：Auzou、Rips、Derappe、Peyroux

  DOI：——

  日期：——
• PERSONAL CARE COMPOSITION IN A DISSOLVABLE CONTAINER
  申请人：The Dial Corporation

  公开号：US20170156999A1

  公开（公告）日：2017-06-08

  The present disclosure describes a cleansing device. The cleansing device includes a container that is dissolvable in water. The cleansing device also includes a personal care composition. The personal care composition is disposed within the container. When the container dissolves, the personal care composition is to be deposited on a surface.
• Kinetic resolution of acyclic 1,2-diols using a sequential lipase-catalyzed transesterification in organic solvents
  作者：Fritz Theil、Judith Weidner、Sibylle Ballschuh、Annamarie Kunath、Hans Schick

  DOI：10.1021/jo00081a018

  日期：1994.1

  A method for the kinetic resolution of 3-(aryloxy)-1,2-propanediols rac-1a-n without additional protection-deprotection steps using a lipase-catalyzed sequential transesterification with lipase amnno PS has been developed. In the first step of this one-pot procedure the racemic 1,2-diols are acylated regioselectively at the primary hydroxy group without enantioselection. The subsequent acylation at the secondary hydroxy group of the formed primary monoacetate is responsible for high enantioselection. The enantioselectivity of this transformation depends significantly on the substitution pattern of the aryl ring and the organic solvent used. 3-(Aryloxy)-1,2-propanediols with substituents in the para-position show a much higher enantioselectivity than the corresponding derivatives with ortho-substituents. Among other substrates, the pharmaceuticals Mephenesin, Guaifenesin, and Chlorphenesin have been resolved. The replacement of the aryloxy by alkyl substituent causes a dramatic decrease of enantioselectivity.
• 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。