3-hydroxypropyl 2-phenylethanoate | 132088-02-9

• 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: 3-hydroxypropyl 2-phenylethanoate
• 英文别名: 3-hydoxypropyl-2-phenylethanoate；phenyl-acetic acid-(3-hydroxy-propyl ester)；Phenyl-essigsaeure-(3-hydroxy-propylester)；3-Hydroxypropyl 2-phenylacetate
• CAS: 132088-02-9
• 化学式: C₁₁H₁₄O₃
• 分子量: 194.23
• InChiKey: OEGJDPOLCIXYOT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  苯乙醛 在 碘 、 对甲苯磺酸 、 mercury(II) oxide 作用下， 以 苯 为溶剂， 反应 10.0h， 生成 3-hydroxypropyl 2-phenylethanoate
  参考文献：
  名称：

  Suginome, Hiroshi; Wang, Jian Bo, Journal of the Chemical Society. Perkin transactions I, 1990, # 10, p. 2825 - 2829

  摘要：

  DOI：

文献信息

• Four acid-catalysed dehydration reactions proceed without interference
  作者：Rio Carlo Lirag、Ognjen Š. Miljanić

  DOI：10.1039/c4cc02990a

  日期：——

  Four acid-catalysed dehydration reactions can proceed in one pot, simultaneously and without interference, to yield one imine, one acetal (or boronic ester), one ester and one alkene, even though many other cross-products could be conceived. This advanced self-sorting behaviour is attributed to different dehydration rates, brought about by dissimilar electronic properties of starting materials.

  即使可以设想许多其他交叉产物，也可以在一个反应​​釜中同时进行四个酸催化的脱水反应，而不会产生干扰，从而生成一种亚胺，一种乙缩醛（或硼酸酯），一种酯和一种烯烃。这种先进的自选行为归因于不同的脱水速率，这是由起始原料的不同电子特性引起的。
• 2-Iodoxybenzoic Acid/Tetraethylammonium Bromide/Water: An Efficient Combination for Oxidative Cleavage of Acetals
  作者：Chutima Kuhakarn、Waraporn Panchan、Supanimit Chiampanichayakul、Natthapol Samakkanad、Manat Pohmakotr、Vichai Reutrakul、Thaworn Jaipetch

  DOI：10.1055/s-0028-1087986

  日期：——

  acyclic acetals to the corresponding hydroxyalkyl carboxylic esters and simple esters, respectively. 2-Iodoxybenzoic acid (IBX) in the presence of tetraethylammonium bromide was employed for the reaction in aqueous media. The salient features of the protocol include short reaction time, environmentally benign reagents and solvent, and moderate to high yields. o-iodoxybenzoic acid - acetals - oxidations

  已经开发出一种简单有效的方法，用于将环状和非环状缩醛分别氧化为相应的羟烷基羧酸酯和简单酯。在四乙基溴化铵存在下，将2-碘氧基苯甲酸（IBX）用于水性介质中的反应。该方案的显着特征包括反应时间短，对环境无害的试剂和溶剂以及中等至高产率。 邻碘氧苯甲酸-缩醛-氧化-羟烷基酯-醇
• Ketene Acetals. XIX. 2-Methylene-1,3-dioxolanes and 1,3-Dioxanes
  作者：S. M. McElvain、Michael J. Curry

  DOI：10.1021/ja01191a071

  日期：1948.11
• NOVEL SULFAMATE COMPOUND CONTAINING N-SUBSTITUTED CARBAMOYL GROUP AND METHOD FOR PREPARING THE SAME
  申请人：YUKONG LIMITED

  公开号：EP0801642B1

  公开（公告）日：2000-12-20
• Facile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in water
  作者：Waraporn Panchan、Supanimit Chiampanichayakul、Deanna L. Snyder、Siriporn Yodbuntung、Manat Pohmakotr、Vichai Reutrakul、Thaworn Jaipetch、Chutima Kuhakarn

  DOI：10.1016/j.tet.2010.01.098

  日期：2010.4

  The combination of (diacetoxy)iodobenzene (Phl(OAc)(2), DIB) and lithium bromide (LiBr) efficiently oxidized cyclic and acyclic acetals to the corresponding hydroxyalkyl carboxylic esters and simple esters in good to excellent yields The merits of this reaction are that it employs commercially available and non-explosive hypervalent iodine(III) reagent, water as the solvent, a short reaction tune, and mild reaction conditions (C) 2010 Elsevier Ltd All rights reserved