Introduction

Spilanthol (1), or (2E,6Z,8E)-N-isobutyl-2,6,8-decatrienamide, is a naturally occurring N-alkylamide found in various medicinal plants, notably Heliopsis longipes, widely used in traditional remedies across the globe. Structurally, spilanthol features an unsaturated amide and a conjugated diene system, rendering it an intriguing compound for Diels–Alder cycloaddition reactions. Its use as a renewable scaffold opens a sustainable route for the synthesis of structurally diverse, potentially bioactive heterocycles, contributing to the advancement of green synthetic methodologies.

Methods

Spilanthol (1) was extracted from dried roots of H. longipes via ethanol maceration and purified by column chromatography. Cycloaddition reactions were performed using various dienophiles (1.2 equiv) in suitable solvents (0.2 mM concentration). A range of Brønsted and Lewis acids was evaluated as catalysts. TLC monitored reaction progress, and the crude products were purified by flash chromatography.

Results

A variety of dienophiles, including aldehydes and succinimides, were tested. Among the catalysts screened, only BF₃·OEt₂ effectively promoted the formation of the desired [4+2] cycloadduct. Neither thermal conditions nor other Lewis acids yielded the product, often resulting in decomposition or no reaction. The use of BF₃·OEt₂ yielded a pyran derivative in moderate isolated yield. NMR confirmed the product's structure.

Conclusions

This work highlights spilanthol (1) as a promising, bio-based diene for Diels–Alder chemistry. The use of BF₃·OEt₂ as a promoter enables efficient, one-step access to heterocyclic scaffolds from renewable plant resources. These findings underscore the potential of natural alkamides in green synthetic strategies and their relevance in the development of novel pharmacophores from biomass-derived starting materials.