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    焦家俊, 韩海军, 侯钰暄, 王静. 5-氯-2-(4-氯-苯氧基)-苯酚的合成[J]. 华东理工大学学报(自然科学版), 2007, (1): 75-78.
    引用本文: 焦家俊, 韩海军, 侯钰暄, 王静. 5-氯-2-(4-氯-苯氧基)-苯酚的合成[J]. 华东理工大学学报(自然科学版), 2007, (1): 75-78.
    JIAO Jia-jun, HAN Hai-jun, HOU Yu-xuan, WANG Jing. Synthetic Process of Active Antimicrobial 5-Chloro-2-(4-Chloro-Phenoxy)-Phenol[J]. Journal of East China University of Science and Technology, 2007, (1): 75-78.
    Citation: JIAO Jia-jun, HAN Hai-jun, HOU Yu-xuan, WANG Jing. Synthetic Process of Active Antimicrobial 5-Chloro-2-(4-Chloro-Phenoxy)-Phenol[J]. Journal of East China University of Science and Technology, 2007, (1): 75-78.

    5-氯-2-(4-氯-苯氧基)-苯酚的合成

    Synthetic Process of Active Antimicrobial 5-Chloro-2-(4-Chloro-Phenoxy)-Phenol

    • 摘要: 以对二氯苯为起始原料,经过乙酰基化、醚化、过氧乙酸氧化、水解得到5-氯-2-(4-氯-苯氧基)-苯酚,改良后的工艺使终产品收率达32.9%,醚化反应改用氢氧化钾代替碳酸钾与对氯苯酚反应制备亲核试剂,均三甲苯代替二甲苯为溶剂,醚化产物收率达到69.2%。氧化反应使用乙酸酐与过氧化氢(w=0.30)反应制备氧化剂,乙酸为溶剂,氧化反应收率达到72.7%。

       

      Abstract: This paper presents an improved process for the synthesis of 5-chloro-2-(4-chloro-phenoxy)-phenol by using 1,4-dichlorobenzene as a starting material,through acetylation,etherification,acetylperoxide oxidation and hydrolysis,the total yield reached 32.9%.Mesitylene instead of xylene,was used as solvent,and potassium hydroxide instead of potassium carbonate,was used to react with phenol to generate nucleophilic reagent during etherization,through which the yield reached 69.2%.During the acetylperoxide oxidation,with acetic acid as solvent,peracetiacid as oxidizing agent prepared through the reaction of acetic anhydride with hydrogen peroxide(w=0.30),the yield reached 72.7%.

       

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