Selective catalytic synthesis of new terpenic chlorides using NaDCC as an eco-friendly and highly stable FAC agent.

Abstract

A simple, mild and efficient scope pathway for a selective catalytic chlorination of terpenic olefins is investigated in the presence of a highly efficient chlorination agent and a readily available Lewis acid catalyst. The sodium dichloroisocyanurate (NaDCC) used in the present work as an easy handling, sustainable and cost-effective chlorine donor due to its high free available chlorine (FAC), exhibits a high efficiency for selective catalytic chlorination. Herein, we report for the first-time the FeCl2/NaDCC combination system for the selective catalytic chlorination towards new functionalized terpenic olefins. In order to examine the general features of this catalytic reaction, the effects of pH, solvent, dilution, chlorination agent nature, stoichiometry and reaction kinetics are optimized using carvone as a model substrate. Among the studied parameters, catalyst stoichiometry was found to be determinant for highly controllable chlorination selectivity towards new allylic and vinylic chlorides. Indeed, the oxidation state, ligand and metal effects of the catalyst are examined using various Lewis acids, where the chlorinated ones (MClx), such as FeCl2, FeCl3 and SnCl2, exhibit a comprehensive approach for a controllable chlorination reaction. In addition, the homogeneous catalytic system shows good reusability with significant catalytic conversion depending on the FAC content in the reaction medium. The reaction proceeds under mild conditions with shorter reaction time and high selectivity towards new high added value allylic and vinylic chlorinated derivatives of naturally occurring terpenic olefins in good to excellent yields.