氯化苄基三乙铵催化2-呋喃乙腈的苄基化反应  

Benzylation of 2-furylacetonitrile Using Benzyltriethylammonium Chloride Catalysis

作　　者：盛继文[1] 刘冬梅[2] 王思宏[3] 田官荣[3] 李耀辉[1] 张普庆[1] 

机构地区：[1]潍坊医学院化学教研室,山东潍坊261042 [2]潍坊医学院药学教研室,山东潍坊261042 [3]延边大学化学系,吉林延吉133002

出　　处：《长春师范学院学报（自然科学版）》2007年第3期49-50,共2页Journal of Changchun Teachers College

摘　　要：以NaOH作为碱,在相转移催化剂氯化苄基三乙铵的存在下,2-呋喃乙腈与苄基溴发生苄基化反应,得到了α-苄基-2-呋喃乙腈和α,α-二苄基-2-呋喃乙腈。The benzylation was taken place between 2-furylacetonitrile and benzyl bromide, а - benzyl - 2-furylacetonitrile and а, а-dibenzyl - 2-furylacetonitrile were obtained under the conditions of benzyltriethylanmmonium chlolide as phase transfer catalyst and sodium hydroxide as base.

关 键 词：相转移催化 苄基化 氯化苄基三乙铵 2-呋喃乙腈 α-苄基-2-呋喃乙腈 α α-二苄基-2-呋喃乙腈 

分 类 号：O621[理学—有机化学]