Alkylation of 1-phenyl-3,5-disubstituted pyrazoles with polyfluorinated aliphatic aldehydes: Properties of 1-phenyl-4-(1-hydroxypolyfluoroalkyl)pyrazole derivatives

Y. G. Shermolovich, S. V. Yemets

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Polyfluorinated aliphatic aldehydes react with 1-phenyl-3-methylpyrazole-5-one, 1-phenyl-3-methyl-5-amino (N, N-dimethylaminomethylenamino)pyrazole and 1-phenyl-3-aminopyrazole-5-one at room temperature in the absence of catalyst with formation of 4-(1-hydroxypolyfluoroalkyl)pyrazoles. Dehydration of 4-(1-hydroxypolyfluoroalkyl)pyrazoles with morpholinosulfur trifluoride generates 4-polyfluoroalkylidenepyrazoles, which are active dienophiles and react with 2,3-dimethylbutadiene and cyclopentadiene forming spirocyclic pyrazole derivatives.

Original languageEnglish (US)
Pages (from-to)111-116
Number of pages6
JournalJournal of Fluorine Chemistry
Volume101
Issue number1
DOIs
StatePublished - Jan 2000

Keywords

  • Alkylation
  • Polyfluorinated aliphatic aldehyde
  • Pyrazole

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