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一种温和的催化氧化体系:用于环己烯二羟基化反应的FePcOTf/H₂O₂

A Mild Catalytic Oxidation System: FePcOTf/H2O2 Applied for Cyclohexene Dihydroxylation.

作者信息

Zhou Baocheng, Chen Wenxing

机构信息

Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, China.

Key Laboratory of Advanced Textile Materials and Manufacturing Technology, Ministry of Education of China, Zhejiang Sci-Tech University, Hangzhou 310018, China.

出版信息

Molecules. 2015 May 11;20(5):8429-39. doi: 10.3390/molecules20058429.

DOI:10.3390/molecules20058429
PMID:25970042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6272422/
Abstract

Iron (III) phthalocyanine complexes were employed for the first time as a mild and efficient Lewis acid catalyst in the selective oxidation of cyclohexene to cyclohexane-1,2-diol. It was found that the catalyst FePcOTf shown excellent conversion and moderate selectivity relative to other iron (III) phthalocyanine complexes. The optimum conditions of the oxidation reaction catalyzed by FePcOTf/H2O2 have been researched in this paper. Iron (III) phthalocyanine triflate (1 mol %) as catalyst, hydrogen peroxide as oxidant, methanol as solvent, and a mole ratio of substrate and oxidant (H2O2) of 1:1 were used for achieving moderate yields of 1,2-diols under reflux conditions after eight hours.

摘要

首次将铁(III)酞菁配合物用作温和且高效的路易斯酸催化剂,用于将环己烯选择性氧化为环己烷 - 1,2 - 二醇。研究发现,相对于其他铁(III)酞菁配合物,催化剂FePcOTf表现出优异的转化率和适度的选择性。本文研究了FePcOTf/H₂O₂催化氧化反应的最佳条件。以三氟甲磺酸铁(III)酞菁(1 mol%)为催化剂,过氧化氢为氧化剂,甲醇为溶剂,底物与氧化剂(H₂O₂)的摩尔比为1:1,在回流条件下反应八小时,可获得适度产率的1,2 - 二醇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/dd8a3b76b247/molecules-20-08429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/c1c1ad590731/molecules-20-08429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/f04b553cf94a/molecules-20-08429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/dd8a3b76b247/molecules-20-08429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/c1c1ad590731/molecules-20-08429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/f04b553cf94a/molecules-20-08429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/600d/6272422/dd8a3b76b247/molecules-20-08429-g003.jpg

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