One-pot synthesis yields grapevine moth sex pheromone | Chemical & Engineering News
Latest News
Web Date: September 14, 2017

One-pot synthesis yields grapevine moth sex pheromone

Ecofriendly vineyard pest control made more efficiently by new process
Department: Science & Technology
News Channels: Biological SCENE, Organic SCENE
Keywords: Synthesis, moth, sex pheromone, Lobesia botrana, Grignard reagent, iron catalyst, pesticide, grapes, wine, vineyard
[+]Enlarge
The European grapevine moth lays its eggs on vineyard grapes. The caterpillars eat the grapes, turn the juice acidic, and provide a toehold for fungal rot.
Credit: Sarah McCaffrey/Museum Victoria
Photo of European grapevine moth, <italic>Lobesia botrana</italic>.
 
The European grapevine moth lays its eggs on vineyard grapes. The caterpillars eat the grapes, turn the juice acidic, and provide a toehold for fungal rot.
Credit: Sarah McCaffrey/Museum Victoria

The European grapevine moth (Lobesia botrana) spoils vineyard fruit across the globe. One of the most effective weapons against the widespread pest is the moth’s own sex pheromone. When sprayed into the air around the grapevines, it leads males on a fruitless chase to find females, disrupting mating. However, the pheromone is about 60% more expensive than traditional pesticides. Now, a partnership of industrial and academic researchers has come up with a less costly one-pot synthesis and is making the pheromone on an industrial scale (Org. Process Res. Dev.2017, DOI: 10.1021/acs.oprd.7b00206).

Sex pheromones make excellent compounds for ecofriendly pest control because they target particular insects and pose no risk to humans or other beneficial insects. But the European grapevine moth pheromone, (7E,9Z)-dodecadien-1-yl acetate, is expensive. The standard synthetic route to the pheromone starts with a pricey eight-carbon compound and requires isolating four intermediates. The process yield is only 11% with 80% isomeric purity.

Olivier Guerret, head of biocontrol and vice president at M2i Life Sciences, helped devise a new and simpler synthesis based on a cross-coupling reaction between a dienol phosphate and a Grignard reagent. Often, such a coupling requires expensive palladium catalysts. However, Guerret collaborated with Gérard Cahiez of Chimie ParisTech, who knew how to replace palladium catalysts with less expensive iron ones. Their two-step route starts with cheaper six-carbon backbones, proceeds all in one pot, and has an 85% yield with 80% isomeric purity.

M2i is now selling raw pheromone to distributors. The researchers have since improved the isomeric purity beyond what they reported and are working on a microencapsulated product that gradually releases pheromone when sprayed on grapevines. That formulation should cost the same as conventional pesticides, Guerret says.

 
Chemical & Engineering News
ISSN 0009-2347
Copyright © American Chemical Society

Leave A Comment

*Required to comment