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3-氟-4-硝基苯酚的合成
引用本文:张天永,夏文娟,王昭,池立峰,卢洲.3-氟-4-硝基苯酚的合成[J].精细化工,2008,25(5):505-508.
作者姓名:张天永  夏文娟  王昭  池立峰  卢洲
作者单位:天津大学,化工学院,精细化工系,天津,300072
摘    要:研究了含氟中间体3-氟-4-硝基苯酚(FNP)的合成,由间氟苯胺经重氮化、水解、硝化及异构体分离制得。间氟苯胺重氮盐在CuSO4和硫酸介质中,用反应蒸馏技术,水解制得间氟苯酚,收率85%,质量分数95%;间氟苯酚硝化后采用水蒸气蒸馏法,把副产物3-氟-6-硝基苯酚有效除去,再经乙醚萃取、饱和NaCl水溶液洗涤、饱和NaHCO3水溶液洗涤、Na2CO3水溶液中和成盐、酸化、乙醚萃取等后处理,得到质量分数99.6%的FNP,收率23%。

关 键 词:3-氟-4-硝基苯酚  间氟苯胺  间氟苯酚  硝化  重氮化  精细化工中间体
文章编号:1003-5214(2008)05-0505-04
修稿时间:2007年12月17

Synthesis of 3-Fluoro-4-nitrophenol
ZHANG Tian-yong,XIA Wen-juan,WANG Zhao,CHI Li-feng,LU Zhou.Synthesis of 3-Fluoro-4-nitrophenol[J].Fine Chemicals,2008,25(5):505-508.
Authors:ZHANG Tian-yong  XIA Wen-juan  WANG Zhao  CHI Li-feng  LU Zhou
Abstract:3-Fluoro-4-nitrophenol(FNP),an important fluoric intermediate,was synthesized from m-fluoroaniline by a four-step way including diazotization,hydrolysis,nitration and separation of the isomers.The diazonium salt of m-fluoroaniline was hydrolyzed by the technology of reaction distillation in the solution of CuSO4 and H2SO4 to give m-fluorophenol in 85% yield and of 95% purity.After nitration of m-fluorophenol,steam distillation was used to remove the by-product 3-fluoro-6-nitrophenol,then the residual bottom liquid was extracted with Et2O.The Et2O layer was washed with saturated aqueous NaCl and NaHCO3,and poured to a solution of Na2CO3.The precipitated sodium salt of FNP was dissolved in water,acidified,extracted by Et2O and evaporated to give FNP in 23% yield and of 99.6% purity.
Keywords:3-fluoro-4-nitrophenol  m-fluoroaniline  m-fluorophenol  nitration  diazotization  fine chemical intermediates
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