β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water

陈鸿雁; 纪红兵

doi:10.1016/S1004-9541(11)60079-7

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β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water

Updated：2026-01-06

- β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water
- β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water
- 中国化学工程学报（英文版） 2011年19卷第6期页码：972-977
- Affiliations：
  
  1. School of Chemistry and Chemical Engineering, the Key Laboratory of Low-carbon Chemistry & Energy Conservation of Guangdong Province, Sun Yat-sen University,Guangzhou,China,510275
  2. Department of Chemical Engineering, Huizhou University,Huizhou,China,516007
- Author bio：
- Funds：
  
  Supported by the National Natural Science Foundation of China (21036009,21176268);the Higher-level Talent Project for Guangdong Provincial Universities and the Fundamental Research Funds for the Central Universities
- DOI：10.1016/S1004-9541(11)60079-7
  中图分类号：
- 纸质出版：2011
- Accepted：
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陈鸿雁, 纪红兵. β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water[J]. 中国化学工程学报（英文版）, 2011,19(6):972-977.

CHEN Hongyan, JI Hongbing. β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water[J]. , 2011, 19(6): 972-977.
陈鸿雁, 纪红兵. β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water[J]. 中国化学工程学报（英文版）, 2011,19(6):972-977. DOI： 10.1016/S1004-9541(11)60079-7.

CHEN Hongyan, JI Hongbing. β-Cyclodextrin Promoted Oxidation of Cinnamaldehyde to Natural Benzaldehyde in Water[J]. , 2011, 19(6): 972-977. DOI： 10.1016/S1004-9541(11)60079-7.

摘要

Abstract

A facile and efficient procedure has been developed systematically for the oxidative cleavage of cinnamaldehyde to benzaldehyde by sodium hypochlorite with water as the only solvent in the presence of β-cyclodextrin (abbreviated as β-CD). Different factors influencing cinnamaldehyde oxidation

e.g

. reaction temperature

the amount of catalyst and oxidant

have been investigated. The yield of benzaldehyde reaches 76% under the optimum conditions (333 K

4 h

molar ratio of cinnamaldehyde to β-CD is 1:1). Furthermore

a feasible reaction mechanism including the formation of benzaldehyde and the two main byproducts (phenylacetaldehyde and epoxide of cinnamaldehyde) has been proposed.

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