丙酮氰醇为氰源的卤代烃的氰基取代反应研究  

Study on the Cyanide Substitution Reaction of Acetone Cannolhydrin as Cyanogen Source

作　　者：郭芳 由君 武文菊 喻艳超 井彬 刘波[1] Guo Fang;You Jun;Wu Wenju;Yu Yanchao;Jing Bin;Liu Bo(Key Laboratory of Green Chemical Engineering and Technology of Heilongjiang Province,College of Materials Science and Engineering,Harbin University of Science and Technology,Harbin,150040)

机构地区：[1]哈尔滨理工大学材料科学与工程学院绿色化工技术黑龙江省高校重点实验室,哈尔滨150040

出　　处：《有机化学》2021年第5期1968-1973,共6页Chinese Journal of Organic Chemistry

基　　金：黑龙江省自然科学基金(No.LH2019B010);国家自然科学基金(Nos.21908034,22008045)资助项目.

摘　　要：氰基取代反应是有机合成中引入氰基官能团的重要方法.以丙酮氰醇为氰化试剂,以脂肪族卤代烷R—X(X=Cl,Br,I)为底物,通过亲核取代反应合成一系列氰基化合物.研究结果表明,在50℃下四氢呋喃(THF)与1,3-二甲基咪唑啉酮(DMI)(体积比为3∶1)组成的混合物为反应溶剂,LiOH•H2O为碱,丙酮氰醇与相应的卤代烷反应可以得到氰化产物,产率达到70%~99%.该反应使用廉价低毒的丙酮氰醇替代剧毒的氰化钠或其他价格昂贵、使用条件苛刻的氰化试剂,且不需要贵金属作催化剂,反应条件温和,适用范围广泛,具有较大的应用价值.The cyano substitution reaction is an important method for introducing cyano functional groups in organic synthesis.In this paper,a series of cyano compounds were synthesized by nucleophilic substitution reaction using acetone cyanohydrin as cyanation reagent and aliphatic haloalkanes R—X(X=Cl,Br,I)as substrates.The results show that the cyanation product can be obtained by reacting the acetone cyanohydrin with the corresponding halogenated alkanes at 50℃,and the yield can reach 70%~99%.The reaction solvent is the mixture of tetrahydrofuran(THF)and 1,3-dimethylimidazolinone(DMI)(volume ratio of 3∶1),and the base is LiOH•H2O.This reaction uses cheap and low toxicity acetone cyanohydrin instead of highly toxic sodium cyanide or other expensive cyanide reagents requiring harsh conditions and it also does not require precious metals as catalysts.The reaction conditions is mild so that it has extensive application and great value of practical application.

关 键 词：卤代烷 丙酮氰醇 氰基取代反应 氰化产物 

分 类 号：TQ226.61[化学工程—有机化工]