1-苯基-2-吡咯烷酮的合成  

Preparation of 1-Phenyl-2-pyrrolidinone

作　　者：张志德[1] 陈玉琴[1] 林凤珍[1] 孟德素[1] 

机构地区：[1]山东师范大学化学化工与材料科学学院,山东济南250014

出　　处：《精细化工》2004年第11期869-871,共3页Fine Chemicals

基　　金：山东省自然科学基金资助项目(Q98B02118)~~

摘　　要：以磷酸作催化剂,γ 丁内酯与苯胺反应合成了1 苯基 2 吡咯烷酮,确定了反应的最佳工艺条件:n(γ 丁内酯)∶n(苯胺)∶n(磷酸)=1 0∶1 5∶0 1,反应时间2h,反应温度为180～210℃;产物经减压蒸馏、重结晶分离提纯,过量苯胺经蒸馏、分水后回收,蒸馏后的残余物作催化剂循环使用,1 苯基 2 吡咯烷酮收率为96 2%,质量分数99 5%;产品用元素分析、红外、核磁进行了确证。1-Phenyl-2-pyrrolidinone was prepared from γ-butyrolactone and aniline catalyzed by phosphoric acid.The optimal process conditions were:n(γ-butyrolactone)∶n(aniline)∶n(phosphoric acid)=1.0∶1.5∶0.1,reaction temprature 180～210 ℃ and reaction time 2 h.The product was purified by vacuum distillation and recrystallization.Aniline was recovered by distillation and seperated from water,and the residue as catalyst was reused.Yield of 1-phenyl-2-pyrrolidinone was 96.2% with 99.5% purity.The product was certified by elementary analysis,IR and^1HNMR.

关 键 词：1-苯基-2-吡咯烷酮 Γ-丁内酯 苯胺 

分 类 号：TQ235[化学工程—有机化工]