Uncatalyzed aerobic epoxidation of liquid alkyl alkenes
Researchers have investigated for decades a suitable catalyst to selectively synthesize epoxides from alkenes with air. Here we show that a selective aerobic epoxidation of industrial alkyl alkenes in liquid phase occurs without any catalyst, solvent nor additive, just placing the neat alkene under 3-5 bar of O<sub>2</sub> and heating between 100 and 200 °C. The reaction can be performed in either an autoclave, a stirring vessel with air bubbling or even a simple open flask, provided that any metal piece is not in contact with the reaction. Alkyl epoxides are directly obtained, after air venting, in yields and selectivity up to 90%. The simplicity of the set-up (just the neat liquid alkene and air) allows to engage the epoxidation reaction with either a previous alkene formation (upstreaming) or a later epoxide opening (downstreaming) reactions, to achieve a variety of industrially-relevant organic products in one-pot.
Authors
- Judit Oliver–Meseguer (ORCID: https://orcid.org/0000-0003-1555-3583)
- Francisco Garnes–Portolés
- Antonio Leyva‐Pérez (ORCID: https://orcid.org/0000-0003-1063-5811)
- Silvia Rodríguez‐Nuévalos
- Susi Hervàs−Arnandis
Institutions
- Instituto de Tecnología Química (ES)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-07-16
- DOI
- https://doi.org/10.1038/s41467-025-61711-3
- Citations
- 4
- Primary Topic
- Catalysis and Oxidation Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.56
Funders
- Generalitat Valenciana
- Universitat Politècnica de València
- Agencia Estatal de Investigación
- Agència Valenciana de la Innovació