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醇直接氧化酯化的高效简便方法。

Efficient and simple approaches towards direct oxidative esterification of alcohols.

作者信息

Ray Ritwika, Jana Rahul Dev, Bhadra Mayukh, Maiti Debabrata, Lahiri Goutam Kumar

机构信息

Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai, 400 076 (India).

出版信息

Chemistry. 2014 Nov 17;20(47):15618-24. doi: 10.1002/chem.201403786. Epub 2014 Oct 3.

DOI:10.1002/chem.201403786
PMID:25284591
Abstract

The present article describes novel oxidative protocols for direct esterification of alcohols. The protocols involve successful demonstrations of both "cross" and "self" esterification of a wide variety of alcohols. The cross-esterification proceeds under a simple transition-metal-free condition, containing catalytic amounts of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy)/TBAB (tetra-n-butylammonium bromide) in combination with oxone (potassium peroxo monosulfate) as the oxidant, whereas the self-esterification is achieved through simple induction of Fe(OAc)2 /dipic (dipic=2,6-pyridinedicarboxylic acid) as the active catalyst under an identical oxidizing environment.

摘要

本文描述了用于醇直接酯化的新型氧化方法。这些方法成功展示了多种醇的“交叉”和“自身”酯化反应。交叉酯化反应在简单的无过渡金属条件下进行,该条件包含催化量的TEMPO(2,2,6,6-四甲基-1-哌啶氧基)/TBAB(四正丁基溴化铵),并以过一硫酸钾(oxone)作为氧化剂,而自身酯化反应是在相同的氧化环境下,通过简单引入Fe(OAc)₂ /dipic(dipic = 2,6-吡啶二甲酸)作为活性催化剂来实现的。

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