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.

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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

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article

Uncatalyzed aerobic epoxidation of liquid alkyl alkenes

Judit Oliver–Meseguer, Francisco Garnes–Portolés, Antonio Leyva‐Pérez, Silvia Rodríguez‐Nuévalos et al.
4 citations
Nature Communications
Catalysis and Oxidation Reactions
1.56
article

Uncatalyzed aerobic epoxidation of liquid alkyl alkenes

Judit Oliver–Meseguer, Francisco Garnes–Portolés, Antonio Leyva‐Pérez, Silvia Rodríguez‐Nuévalos, Susi Hervàs−Arnandis
article en
4 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
Instituto de Tecnología Química (ES)
Generalitat Valenciana, Universitat Politècnica de València, Agencia Estatal de Investigación, Agència Valenciana de la Innovació
Openalex Percentile: Top 17%
Catalysis and Oxidation Reactions
1.56
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Uncatalyzed aerobic epoxidation of liquid alkyl alkenes — Judit Oliver–Meseguer, Francisco Garnes–Portolés, et al. · Nature Communications (2025) | TGRS Research Map | TGRS