{"title":"钌络合催化剂选择性氧化乙醇醛制乙二醛。","authors":"Takuya Sagawa, Atsushi Kondo, Mineo Hashizume","doi":"10.1002/cplu.202500616","DOIUrl":null,"url":null,"abstract":"<p><p>Cellulose comprises glucose units, and therefore glucose and its derivatives have received attention as a carbon source replacing fossil fuels. In particular, glyoxal, which is obtained from glucose by retro-aldol reaction and subsequent oxidation via glycolaldehyde, is a feedstock for useful chemicals. However, efficient catalytic synthesis of glyoxal from glycolaldehyde has not been reported because the unwanted excessive oxidation of glyoxal occurs. In this study, catalytic synthesis of glyoxal from glycolaldehyde using a ruthenium complex catalyst with a bromophenyl terpyridine ligand was carried out. After optimizing reaction conditions, glyoxal was obtained in a 32% yield in N,N-dimethylformamide at 100°C for 3 h using O<sub>2</sub> gas as an oxidant. Furthermore, the obtained mixture was reacted with sodium sulfite to form precipitates, which are bisulfite adducts. It could be easily separated as a glyoxal equivalent from the catalyst and solvent by filtration. These results indicate that a new method for the synthesis of glyoxal from biomass-derived glycolaldehyde has been achieved.</p>","PeriodicalId":148,"journal":{"name":"ChemPlusChem","volume":"91 5","pages":"e202500616"},"PeriodicalIF":2.8000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13130154/pdf/","citationCount":"0","resultStr":"{\"title\":\"Selective Oxidation of Glycolaldehyde to Glyoxal Using Ruthenium Complex Catalysts.\",\"authors\":\"Takuya Sagawa, Atsushi Kondo, Mineo Hashizume\",\"doi\":\"10.1002/cplu.202500616\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cellulose comprises glucose units, and therefore glucose and its derivatives have received attention as a carbon source replacing fossil fuels. In particular, glyoxal, which is obtained from glucose by retro-aldol reaction and subsequent oxidation via glycolaldehyde, is a feedstock for useful chemicals. However, efficient catalytic synthesis of glyoxal from glycolaldehyde has not been reported because the unwanted excessive oxidation of glyoxal occurs. In this study, catalytic synthesis of glyoxal from glycolaldehyde using a ruthenium complex catalyst with a bromophenyl terpyridine ligand was carried out. After optimizing reaction conditions, glyoxal was obtained in a 32% yield in N,N-dimethylformamide at 100°C for 3 h using O<sub>2</sub> gas as an oxidant. Furthermore, the obtained mixture was reacted with sodium sulfite to form precipitates, which are bisulfite adducts. It could be easily separated as a glyoxal equivalent from the catalyst and solvent by filtration. These results indicate that a new method for the synthesis of glyoxal from biomass-derived glycolaldehyde has been achieved.</p>\",\"PeriodicalId\":148,\"journal\":{\"name\":\"ChemPlusChem\",\"volume\":\"91 5\",\"pages\":\"e202500616\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2026-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13130154/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemPlusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cplu.202500616\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPlusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cplu.202500616","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Selective Oxidation of Glycolaldehyde to Glyoxal Using Ruthenium Complex Catalysts.
Cellulose comprises glucose units, and therefore glucose and its derivatives have received attention as a carbon source replacing fossil fuels. In particular, glyoxal, which is obtained from glucose by retro-aldol reaction and subsequent oxidation via glycolaldehyde, is a feedstock for useful chemicals. However, efficient catalytic synthesis of glyoxal from glycolaldehyde has not been reported because the unwanted excessive oxidation of glyoxal occurs. In this study, catalytic synthesis of glyoxal from glycolaldehyde using a ruthenium complex catalyst with a bromophenyl terpyridine ligand was carried out. After optimizing reaction conditions, glyoxal was obtained in a 32% yield in N,N-dimethylformamide at 100°C for 3 h using O2 gas as an oxidant. Furthermore, the obtained mixture was reacted with sodium sulfite to form precipitates, which are bisulfite adducts. It could be easily separated as a glyoxal equivalent from the catalyst and solvent by filtration. These results indicate that a new method for the synthesis of glyoxal from biomass-derived glycolaldehyde has been achieved.
期刊介绍:
ChemPlusChem is a peer-reviewed, general chemistry journal that brings readers the very best in multidisciplinary research centering on chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies.
Fully comprehensive in its scope, ChemPlusChem publishes articles covering new results from at least two different aspects (subfields) of chemistry or one of chemistry and one of another scientific discipline (one chemistry topic plus another one, hence the title ChemPlusChem). All suitable submissions undergo balanced peer review by experts in the field to ensure the highest quality, originality, relevance, significance, and validity.