ArticleNature communications2025
Coupling nitrate electrochemical reduction and nitrite oxidation of ethanol for acetamide synthesis.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Self-Optimization With Oriented Facet Reconstruction for Universal Electrocatalytic C-N Coupling.Angewandte Chemie (International ed. in English) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Electrochemical acetamide synthesis under ambient conditions offers a sustainable route for converting waste nitrate into valuable chemicals. Conventional methods, limited to standalone reduction or oxidation processes, typically achieve low Faradaic efficiencies (<40%) and yields (<0.2 mmol h⁻¹ cm⁻²). Here, we present a tandem reaction system coupling cathodic reduction and anodic oxidation in a full-cell electrolyzer to enhance acetamide production. At the cathode, nitrate is first reduced to nitrite, which subsequently oxidizes ethanol to acetaldehyde. This acetaldehyde reacts in situ with electrogenerated ammonia to form α-aminoethanol. The intermediate is then transported to the anode, where it undergoes oxidation to yield acetamide. The reaction pathway is confirmed through proton nuclear magnetic resonance spectroscopy, revealing efficient acetamide synthesis with a yield of 7.2 ± 0.3 mmol h⁻¹ (0.45 ± 0.02 mmol h⁻¹ cm⁻²) at a cell voltage of 2.4 V. Furthermore, the strategy extends to other amides, such as formamide and butyramide, underscoring its versatility. Techno-economic analysis highlights the viability of this route, with estimated production costs competitive against conventional thermal processes.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.