5-乙酰基-2-氨基二苯甲酮的超声合成  

Ultrasonic Synthesis of 5-Acetyl-2-aminobenzophenone

作　　者：张学骜[1] 龙永福[1] 谢凯[1] 安立华[1] 

机构地区：[1]国防科技大学光子声子研究中心,湖南长沙410073

出　　处：《精细化工》2003年第10期638-640,共3页Fine Chemicals

基　　金：国家973基金资助项目(51307)

摘　　要：利用超声振荡,以对硝基苯乙酮为原料,在原甲酸三乙酯和对甲苯磺酸的催化作用下和乙二醇醚化保护酮基,然后在氢氧化钠甲醇溶液的碱性条件下和苯乙腈环化加成,再用w(Pd)=5%的Pd-C催化加氢,最后在浓度为1mol/L的高氯酸的强酸作用下恢复酮基,合成出5 乙酰基 2 氨基二苯甲酮,用IR和1HNMR对其结构进行了表征。与非超声合成方法比较,反应时间由44h缩短到32h,目标产物总收率由39 5%提高到69 6%。5Acetyl2aminobenzophenone is synthesized from pnitroacetophenone under the influence of ultrasonic.Firstly,pnitroacetophenone reacted with glycol in the presence of triethyl orthoformate and ptoluenesulfonic acid as catalyst to form ketal for protecting the keto group.Then cyclization was conducted with phenylacetonitrile in an alkaline solution of sodium hydroxide in methanol.In the third step catalytic hydrogenation was carried out using hydrogen gas in the existence of 5% palladium on carbon.Finally 5acetyl2aminobenzophenone was gained under the action of strong acid of 1 mol/L perchloric acid for restoration of the keto group.Structure of the target compound was identified by IR and 1HNMR.Compared with the conventional nonultrasonic synthetic method, the reaction time is shortened from 44 h to 32 h and the the yield of the object product is increased from 395% to 696%.

关 键 词：5-乙酰基-2-氨基二苯甲酮 超声合成 表征 

分 类 号：O625.63[理学—有机化学]