Ultrasound mediated Green Synthesis of Hexa-hydro Triazines

The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation

Abstract-A novel and efficient method has been developed for the synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives by the convenient ultrasound-mediated condensation of 4-hydroxyquinolin-2-one with Meldrum’s acid and aldehydes in the presence of a catalytic amount of [HMIm]HSO4 as a green, efficient and reusable acidic ionic liquid medium. The stability of the ionic liquid during the re...

Direct oxidative coupling of amidine hydrochlorides and methylarenes: TBHP-mediated synthesis of substituted 1,3,5-triazines under metal-free conditions.

Various 2,4,6-trisubstituted 1,3,5-triazines were smoothly formed via TBHP-mediated direct oxidative coupling of amidine and methylarenes. This tandem oxidation-imination-cyclization transformation exhibits a straightforward protocol to prepare 1,3,5-triazines from easily available starting materials and green oxidants under metal-free conditions.

Ultrasound Assisted Green Synthesis and Characterization of Graphene Oxide

   Graphene oxide (GO) was prepared by an improved green chemical method using graphite flakes, KMnO4, a mixture of H2SO4/H3PO4, H2O2 and HCl. In several stages, ultrasound was used to separate the oxidized layers of GO. The use of ultrasound optimizes the effect of the reacting agents, decreasing the required amou...

[BMIm]HSO4 as a Green and Highly Efficient Catalyst for One-pot Synthesis of 3-Substituted Indoles under Ultrasound Irradiation

A practical and green synthesis of 3-substituted indoles is reported via three-component coupling reaction of indoles, aldehydes and N-methylaniline in the presence of the acidic ionic liquid 1-butyl-3-methylimidazolium hydrogen sulfate ([BMIm]HSO4) under ultrasound irradiation at room temperature. The significant features of this procedure are high yields of the products, simple work-up, opera...

SYNTHESIS AND STRUCTURE ELUCIDATION OF 1,2,4-TRIAZINO [4,3-b] 1,2,4-TRIAZINES, 1,2,4-TRIAZINO [3,4-C] 1,2,4-TRIAZINES AND 1,2,4-TRIAZINO [4,3-dl l,2,4-TRIAZINES