Abstract

Among a plethora of known and established oxidant in organic chemistry, hydrogen peroxide stands in a special position. It is commercially and inexpensively available, highly effective, selective, and more importantly it is compatible with current environmental concerns, dictated by principles of green chemistry. Several chemicals or their intermediates that are important in our daily life such as pharmaceuticals, flavors, fragrances, etc. are products of oxidation of alcohols. In this review, we introduce hydrogen peroxide as an effective, selective, green and privileged oxidant for the catalyzed oxidation of primary and secondary benzylic and heterocyclic alcohols to corresponding carbonyl compounds in different media such as aqueous media, under solvent-free conditions, various organic solvent, and dual-phase system.

Highlights

  • Nowadays, energy and environmental crises have resulted in the discovery of green technologies for progressive use in the chemical industry

  • Due to an urgent and important demand for greener approaches, the use of toxic solvents and reagents such as organic peroxides must be avoided. Green solvents such as water or solvent-free systems, clean oxidants such as O2 or H2O2, and recyclable catalysts should be considered in order to comply with the principles of green chemistry proposed by Anastas and Warner [2]

  • We recently reviewed the applications of pyridinium chlorochromate (PCC) as an important selective oxidant for oxidation of primarily and secondary alcohols to their corresponding carbonyl compounds [28]

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Summary

Introduction

Energy and environmental crises have resulted in the discovery of green technologies for progressive use in the chemical industry. Due to an urgent and important demand for greener approaches, the use of toxic solvents and reagents such as organic peroxides must be avoided Green solvents such as water or solvent-free systems, clean oxidants such as O2 or H2O2, and recyclable catalysts should be considered in order to comply with the principles of green chemistry proposed by Anastas and Warner [2]. As a continuation of these interests, we try to highlight the importance and efficacy of hydrogen peroxide as an effective and green oxidant in the catalyzed selective oxidation of primary and secondary benzylic alcohols and primary heterocyclic alcohols to their corresponding carbonyl compounds. We present an overview on the reasonable reaction mechanism and promising catalytic effects of the selective oxidation of alcohols which can be considered as dehydrogenation of alcohols

Oxidation of Benzylic and Heterocyclic Alcohols in Aqueous Media
Entr8y
34 En4t56ry
EEnntt7rryy
21. The selective oxidation of different alcohols a
En4try2-MeC4-6CHlSC4uC6HbHs42tCrOaHHte2OH
Re9action
Fe3O4-ECH-P-5g
En2trEyntry
En3try 4-OM4-eCCl6CSHu6H4bC4sCHtrHa2Ot2eOHH 4-OM4-CeClPC6rH6oHd44CuCHcHtOO
C6H5C4H-O2MOeHC6H4CH2OH
12 FurfuryFluarlfcuorhyol al lcohol
MOR-HC EntrEyn4try CMCaOatatRalyl-yOstsXt
En4try
PyC4 PyCl6
EntC34ry6H5
C6H5CC6HH25OCHH2 4C6H5CH2OH
No reaction
Toluene Solvent
98 COO9H7
En2try C46-HCSl5CuC6bHHs2t4COraHHte2OH
Findings
Conclusions
Full Text
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