Reactivity of 2-benzylpyridyl lithium toward benzonitrile derivatives: Addition versus elimination
作者:Xiaomin Hao、Lu Qin、Mali Xu、Xia Chen
DOI:10.1016/j.jorganchem.2017.10.042
日期:2017.12
hydrolysis product 2-benzylpyridyl-ketone 2–5, respectively, in which the reaction involved in a 1,3-shift of -SiMe3 group to form a dimeric pyridyl-1-aza-allyl-lithium then followed by acidic hydrolysis. The MeOLi elimination reaction between Li2 and p-MeO(C6H4)CN resulted in formation of 4-(2-benzylpyridyl)benzonitrile 6. The reaction of Li2 with p-Me(C6H4)CN in the presence of TMEDA generated a 1:2 hydrolysis
这项工作研究了2-苄基吡啶基锂(2-Pyr)C(Ph)(R)Li(R = SiMe 3,Li1 ; R = H,Li2)对苯甲腈衍生物的反应性。基于不同的产物,锂盐与腈之间的反应可能分别涉及加成,消除和双分子偶联途径。用ArCN(Ar = Ph,p -Tolyl,o -Tolyl,p -OMePh)处理Li1得到加成中间体吡啶基-1-氮杂-烯丙基-锂[(2-Pyr)C(Ph)C(Ar) N(SiMe 3)} Li] 2(1, Ar = Ph)及其相应的水解产物2-苄基吡啶基酮2 –分别参见图5,其中反应涉及-SiMe 3基团的1,3-转移以形成二聚吡啶基-1-氮杂-烯丙基-锂,然后进行酸性水解。之间的MeOLi消除反应LI2和p -MeO(C 6 H ^ 4)CN导致形成4-(2-苄基吡啶基)苄腈6。的反应LI2与p -Me(C 6 H ^ 4)CN在TMEDA的存在下产生的1:2加合物