已经报道了(苯磺酰基)乙腈,芳族醛和6-氨基尿嘧啶的一锅三组分缩合反应,用于制备6,8a-二氢吡啶并[2,3- d ]嘧啶衍生物。该方法涉及多米诺Knoevenagel缩合/迈克尔加成和环化级联。该反应在甘油中进行,甘油是可商购的,廉价且无毒的化合物。产品的高纯度,极高的收率和广泛的底物是该方案的优点。
已经报道了(苯磺酰基)乙腈,芳族醛和6-氨基尿嘧啶的一锅三组分缩合反应,用于制备6,8a-二氢吡啶并[2,3- d ]嘧啶衍生物。该方法涉及多米诺Knoevenagel缩合/迈克尔加成和环化级联。该反应在甘油中进行,甘油是可商购的,廉价且无毒的化合物。产品的高纯度,极高的收率和广泛的底物是该方案的优点。
One-step synthesis of α,β-unsaturated arylsulfones by a novel multicomponent reaction of aromatic aldehydes, chloroacetonitrile, benzenesulfinic acid sodium salt
作者:Lei Zhang、Mao Hua Ding、Hong Yun Guo
DOI:10.1016/j.cclet.2012.10.013
日期:2012.12
Abstract A new and green method for the synthesis of α,β-unsaturated arylsulfones had been achieved through the condensation of aromatic aldehydes, chloroacetonitrile, benzenesulfinic acidsodiumsalt in the presence of 1-butyl-3-methyl imidazolium hydroxide ([bmim]OH) in EtOH under reflux. The ionic liquid was recovered and recycled for subsequent reactions. The advantages of this protocol were non-toxic