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Continuous flow reaction system for the synthesis of 2,2,2-trichloroacetophenone derivatives and its application

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dc.contributor.authorKo, Byeng Ha-
dc.contributor.authorYu, Subeen-
dc.contributor.authorSong, Kwang Ho-
dc.contributor.authorLee, Sunwoo-
dc.date.accessioned2021-09-02T13:47:37Z-
dc.date.available2021-09-02T13:47:37Z-
dc.date.created2021-06-16-
dc.date.issued2018-03-14-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/76735-
dc.description.abstractA continuous flow reaction system was developed for the synthesis of 2,2,2-trichloroacetophenone derivatives. When aryl propiolic acids and water were mixed with trichloroisocyanuric acid in DMF at 5 degrees C, the 2,2,2-trichloroacetophenone derivatives were formed within 5 min with good yields. In addition, the resulting mixture was flowed to react with amines to give the corresponding benzamide. This flow reaction system provided higher yields within shorter times than the batch reaction system. (C) 2018 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectREACTION-TIME CONTROL-
dc.subjectTRICHLOROMETHYL COMPOUNDS-
dc.subjectCHEMISTRY-
dc.subjectOXIDATION-
dc.subjectPRODUCTS-
dc.subjectKETONES-
dc.subjectBATCH-
dc.subjectACID-
dc.titleContinuous flow reaction system for the synthesis of 2,2,2-trichloroacetophenone derivatives and its application-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Kwang Ho-
dc.identifier.doi10.1016/j.tetlet.2018.01.067-
dc.identifier.scopusid2-s2.0-85041517480-
dc.identifier.wosid000427217400007-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.59, no.11, pp.991 - 994-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume59-
dc.citation.number11-
dc.citation.startPage991-
dc.citation.endPage994-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusREACTION-TIME CONTROL-
dc.subject.keywordPlusTRICHLOROMETHYL COMPOUNDS-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusPRODUCTS-
dc.subject.keywordPlusKETONES-
dc.subject.keywordPlusBATCH-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthorFlow chemistry-
dc.subject.keywordAuthorTrichloroacetophenone-
dc.subject.keywordAuthorDecarboxylative chlorination-
dc.subject.keywordAuthorPropiolic acid-
dc.subject.keywordAuthorTrichloroisocyanuric acid-
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