Evidence map›Paper›PMID 42540865›Full record

ArticleRSC advances2026

Synthesis and kinetic modeling of functionalized oxymethylene ethers (f-OMEs) based on lactic acid derivatives and formaldehyde.

Victor Kühnpast, Marius Drexler, Nina Kräber, Falk Rohloff, Thomas A Zevaco, Ulrich Arnold, Jörg Sauer

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Victor KühnpastKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0009-0001-3436-1547
Marius DrexlerKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0000-0001-5457-2790
Nina KräberKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0009-0002-8745-3522
Falk RohloffKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0009-0006-6849-5857
Thomas A ZevacoKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0000-0002-0421-6023
Ulrich ArnoldKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0000-0002-1899-6411
Jörg SauerKarlsruhe Institute of Technology (KIT), Institute of Catalysis Research and Technology (IKFT) Hermann-von-Helmholtz-Platz 1 76344 Eggenstein-Leopoldshafen Germany victor.kuehnpast@kit.edu.ORCID https://orcid.org/0000-0003-3133-4110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to modern civilization's dependence on finite fossil resources, there is a growing need to implement a circular economy. Catalyzed acetalization reactions could contribute to achieve this goal. In such reactions, a wide variety of aldehydes and alcohols can be converted into acetals, which are known for their good recyclability and non-toxicity. Hence, this work focused on the utilization of acetalization reactions to produce novel and facile degradable building blocks for the chemical industry. The educts employed were the lactic acid derivatives ethyl lactate and butyl lactate, as well as formaldehyde, an important C1 bulk chemical that can potentially be produced from green methanol. The synthesis of functionalized oxymethylene ethers (f-OMEs) using the lactic acid derivatives and formaldehyde was performed for the first time. Based on an initial catalyst screening, the cheap and eco-friendly clay material montmorillonite K10 was employed as the catalyst with the highest selectivity for the desired acetals. The different reactivities of the tested solid acid catalysts are discussed. The conversion values reached up to 60%, and the selectivity for f-OMEs reached up to 70%, depending on the reaction conditions. Catalyst screening and experiments covering the relevant reaction conditions were initially carried out in a batch reactor. Subsequently, the process was successfully implemented in a continuously operating fixed-bed reactor, demonstrating the first steps for scale-up and further selectivity control. After a systematic study of the varying reaction conditions, a reaction network was proposed, and a kinetic model to estimate product distributions was developed. The validation of the model showed that the conversion prediction was mostly within a relative deviation of ±30%. The model exhibited good applicability to batch and fixed-bed reactors, making it a useful tool for process upscaling. A solvent-free and scalable production process for f-OMEs was developed, and the novel substances were characterized.

Identifiers

PMID42540865
PMCPMC13426504

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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.