4-苯氧基苯酚的合成改进  

Improvement on Synthesis of 4-Phenoxyphenol

作　　者：高永红[1] 陶建伟[1] 陆庆宁[1] 金东元[1] 

机构地区：[1]上海应用技术学院化工系,上海200235

出　　处：《化学世界》2007年第7期418-420,共3页Chemical World

基　　金：上海市科委重点攻关项目(034319254)

摘　　要：以二苯醚和苯甲酰氯为原料,经酰基化合成4-苯氧基二苯甲酮,然后再经Beayer-villyger氧化以及碱性水解合成4-苯氧基苯酚。主要考察Beayer-villyger氧化反应中反应温度、反应时间、原料配比等因素对产物收率的影响。结果表明,在40°C7、h、n(过氧化氢)∶n(硫酸)∶n(4-苯氧基二苯甲酮)=3.0∶4.0∶1.0条件下,Beayer-villyger氧化反应的收率最高可达91.4%。在上述条件下,经三步反应,得到4-苯氧基苯酚,其总收率达80%以上。经熔点、红外光谱及元素分析确定产物为4-苯氧基苯酚。4-Phenoxyphenol was synthesized from 4-phenoxy-diphenyl ketone prepared with diphenyl ether and benzoyl chloride as raw material through Beayer-villyger reaction and hydrolyzation. The effect of feed composition, reaction time and temperature on Beayer-villyger reaction was investigated. The optimized conditions obtained were： n （H2O2） ： n （H2 SO4）：n （4-phenoxy-diphenyl ketone） = 3.0：4.0 ：1; reaction time, 7 h, temperature, 40 ℃. The yield of Beayer- villyger reaction was 91.4% and the overall yield of 4-phenoxyphenol was about 80%. The products were characterized by IR, elemental analysis and melting point test.

关 键 词：4-苯氧基苯酚 合成 二苯醚 苯甲酰氯 4-苯氧基二苯甲酮 Beayer-villyger氧化 

分 类 号：TQ243.1[化学工程—有机化工]