The nun moth, L. (Linnaeus, 1758), is one of the most important defoliators of coniferous forests in Europe and Asia. In sexual communication, females produce three epoxides and an alkene: (-)-disparlure [(7,8)--7,8-epoxy-2-methyloctadecane], (+)-monachalure [(7,8)--7,8-epoxyoctadecane], (-)-monachalure [(7,8)--7,8-epoxyoctadecane], and their corresponding olefins. This study aimed to develop a green synthesis pathway for all pheromonal components, emphasizing the use of common raw materials, a simplified three-step process, lower costs, and an environmentally friendly approach compared to existing methods. The proposed method introduces a novel synthetic route employing an innovative improvement alkylation step catalyzed by lithium iodide in diglyme. The synthesized compounds were characterized using GC-MS, H NMR, and C NMR spectroscopy. Six synthetic blends were formulated for field testing, with the goal of identifying the most attractive composition. Field trials demonstrated that a blend with a 10:10:1 ratio of (±)-Disparlure, (±)-Monachalure, and ()-2-Methyl-7-octadecene exhibited the highest attraction efficiency.
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