Venkatesan K, Pujari Suresh S, Lahoti R J, Srinivasan K V
Organic Chemistry, Technology Division, National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411 008, India.
Organic Chemistry, Technology Division, National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411 008, India.
Ultrason Sonochem. 2008 Apr;15(4):548-553. doi: 10.1016/j.ultsonch.2007.06.001. Epub 2007 Jun 14.
The condensation reaction involving an aldehyde and diketone was efficiently promoted by the Ionic liquid, [Hbim]BF(4) (IL) as a reaction medium with methanol as co-solvent at ambient temperature under ultrasonic irradiation to afford the corresponding 1,8-dioxo-octahydro-xanthene (xanthene) derivatives in excellent yields. The advantages of this method include among others the use of a recyclable, non-volatile ionic liquid, which promotes this protocol under ambient temperature without the requirement of any added catalyst. The reaction times and yields are compared with p-TSA catalyzed synthesis of xanthenes under thermal conditions, which is also reported for the first time under our reaction conditions.
离子液体[Hbim]BF(4)(IL)作为反应介质,以甲醇为共溶剂,在室温下超声辐射的条件下,能有效地促进醛与二酮的缩合反应,从而以优异的产率得到相应的1,8-二氧代八氢呫吨(呫吨)衍生物。该方法的优点包括使用可回收、不挥发的离子液体,其在室温下促进该反应,无需添加任何催化剂。还将该反应的时间和产率与对甲苯磺酸催化的呫吨热条件下的合成进行了比较,这也是在我们的反应条件下首次报道。