Regioselective synthesis of a branched isomer of nonylphenol, 4-(3′,6′-dimethyl-3′-heptyl)phenol, and determination of its important environmental properties

Joseph O. Lalah, Karl W. Schramm, Dieter Lenoir, Bernhard Henkelmann, Norbert Hertkorn, Georg Matuschek, Antonius Kettrup, Klaus Günther

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

A method for the synthesis of a pure nonylphenol isomer, 4-(3′,6′-dimethyl-3′-heptyl)phenol, by Friedel-Crafts reaction between anisole and 3-bromo-3,6-dimethylheptane that gives a 47.3% overall yield is reported. The reactions were followed by GC-MS, and the chemical structures are in agreement with the NMR and IR spectra. The log Kow value for this compound, its water solubility, vapor pressure, and Henry's Law constant were also determined. These physicochemical properties were required for prediction of the compound's behavior in aquatic ecosystems.

Original languageEnglish
Pages (from-to)4790-4795
Number of pages6
JournalChemistry - A European Journal
Volume7
Issue number22
DOIs
StatePublished - 19 Nov 2001
Externally publishedYes

Keywords

  • Environmental chemistry
  • Friedel-Crafts alkylation
  • Nonylphenol isomer
  • Synthesis design

Fingerprint

Dive into the research topics of 'Regioselective synthesis of a branched isomer of nonylphenol, 4-(3′,6′-dimethyl-3′-heptyl)phenol, and determination of its important environmental properties'. Together they form a unique fingerprint.

Cite this