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Synthesis of Florol via Prins cyclization over heterogeneous catalysts

Eränen Kari; Pérez-Ramírez Javier; Mäki-Arvela Päivi; Sánchez-Velandia Julián E.; Lasne Basile; Kumar Nanendra; Mondelli Cecilia; Peurla Markus; Vajglova Zuzana; Murzin Dmitry Yu; Aho Atte

dc.contributor.authorEränen Kari
dc.contributor.authorPérez-Ramírez Javier
dc.contributor.authorMäki-Arvela Päivi
dc.contributor.authorSánchez-Velandia Julián E.
dc.contributor.authorLasne Basile
dc.contributor.authorKumar Nanendra
dc.contributor.authorMondelli Cecilia
dc.contributor.authorPeurla Markus
dc.contributor.authorVajglova Zuzana
dc.contributor.authorMurzin Dmitry Yu
dc.contributor.authorAho Atte
dc.date.accessioned2022-10-28T13:35:30Z
dc.date.available2022-10-28T13:35:30Z
dc.identifier.urihttps://www.utupub.fi/handle/10024/166065
dc.description.abstractIn this work, several heterogeneous micro- and mesoporous, acidic catalysts were tested for the selective synthesis of Florol (R), an industrial product formed via condensation and rehydration starting from isoprenol and isovaleraldehyde in dimethylcarbonate as a solvent. The results showed that a mildly acidic, microporous H-Beta-300 with SiO2/Al2O3 ratio of 300 was the best catalyst, giving 72% selectivity with 99% conversion at 40 degrees C when using the molar ratio isoprenol to isovaleraldehyde of 1:5. More acidic zeolites gave slightly lower selectivity, while the lowest selectivity (up to 52%) was obtained with mesoporous catalysts exhibiting mild acidity and no strong Bronsted acid sites. Selectivity to pyranols was nearly constant when changing temperature, while a larger excess of isovaleraldehyde promoted formation of tetrahydropyranol. H-Beta-300 catalyst was successfully after calcination at 400 degrees C. DFT calculations pointed out on the parallel formation of tetrahydro pyranols and dihydropyrans, which are the corresponding dehydration products. (C) 2021 Elsevier Inc. All rights reserved.
dc.language.isoen
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.titleSynthesis of Florol via Prins cyclization over heterogeneous catalysts
dc.identifier.urnURN:NBN:fi-fe2022081154873
dc.relation.volume405
dc.contributor.organizationfi=biolääketieteen laitos, yhteiset|en=Institute of Biomedicine|
dc.contributor.organization-code2607100
dc.converis.publication-id174831065
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/174831065
dc.format.pagerange302
dc.format.pagerange288
dc.identifier.eissn1090-2694
dc.identifier.jour-issn0021-9517
dc.okm.affiliatedauthorPeurla, Markus
dc.okm.discipline215 Chemical engineeringen_GB
dc.okm.discipline215 Teknillinen kemia, kemian prosessitekniikkafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeJournal article
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.jcat.2021.12.008
dc.relation.ispartofjournalJournal of Catalysis
dc.year.issued2022


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