Synthesis of furan-2-ones and spirofuran-2,3'-indoline derivatives using polyether sulfone sulfamic acid catalysis
Polyether sulfone sulfamic acid (PES-NHSO3H) was prepared by simple sulfonation of a modified polyether sulfone. The number of acidic sites (SO3H) was determined to be 4.23 mmol H+/g by acid-base titration and 4.29 mmol H+/g by barium sulfate test. PES-NHSO3H was used as an efficient acidic catalyti...
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Veröffentlicht in: | Scientific reports 2024-10, Vol.14 (1), p.26008 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Polyether sulfone sulfamic acid (PES-NHSO3H) was prepared by simple sulfonation of a modified polyether sulfone. The number of acidic sites (SO3H) was determined to be 4.23 mmol H+/g by acid-base titration and 4.29 mmol H+/g by barium sulfate test. PES-NHSO3H was used as an efficient acidic catalytic system for the preparation of functionalized furan-2-ones and 2',5-dioxo-5 H-spiro[furan-2,3 ' -indoline]-3-carboxylate derivatives via the three-component reaction of anilines, aldehydes/1-ethylindoline-2,3-dione, and diethyl acetylene dicarboxylate in high yields (85-97%). The effect of polar and non-polar solvents on the productivity of the reaction was investigated. The catalyst was recovered 11 times without losses in catalytic potential.Polyether sulfone sulfamic acid (PES-NHSO3H) was prepared by simple sulfonation of a modified polyether sulfone. The number of acidic sites (SO3H) was determined to be 4.23 mmol H+/g by acid-base titration and 4.29 mmol H+/g by barium sulfate test. PES-NHSO3H was used as an efficient acidic catalytic system for the preparation of functionalized furan-2-ones and 2',5-dioxo-5 H-spiro[furan-2,3 ' -indoline]-3-carboxylate derivatives via the three-component reaction of anilines, aldehydes/1-ethylindoline-2,3-dione, and diethyl acetylene dicarboxylate in high yields (85-97%). The effect of polar and non-polar solvents on the productivity of the reaction was investigated. The catalyst was recovered 11 times without losses in catalytic potential. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-024-76707-0 |