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2,6-Xylenol

About: 2,6-Xylenol is a research topic. Over the lifetime, 72 publications have been published within this topic receiving 673 citations.


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Patent
Bruce E. Leach1
04 Jun 1979
TL;DR: In this article, a process for preparing 2,6-xylenol in high selectivity and a catalyst composition useful therein are disclosed. The process comprises reacting phenol, o-cresol or mixtures thereof with methanol in presence of water, hydrogen and a catalyzer consisting essentially of Fe 2 O 3, SnO 2, Cr 2 O3, and K 2 O.
Abstract: A process for preparing 2,6-xylenol in high selectivity and a catalyst composition useful therein are disclosed. The process comprises reacting phenol, o-cresol or mixtures thereof with methanol in presence of water, hydrogen and a catalyst consisting essentially of Fe 2 O 3 , SnO 2 , Cr 2 O 3 , and K 2 O.

13 citations

Journal ArticleDOI
TL;DR: In this paper, the effect of the nonpolar field formed by the polymer ligand on the catalysis was studied in dimethyl sulfoxide (DMSO) solvent, and the catalytic activity of the Cu complex increases in the following order; Cu-(styrene-vinylpyridine copolymer) (St·VP) complex > Cu-partially quarternized (by benzyl chloride) poly(vinyl pyridine)(BCQP) complex, etc.
Abstract: The oxidative polymerization catalyzed by Cu(II)-poly(vinylpyridine) derivatives and the effect of the nonpolar field formed by the polymer ligand on the catalysis was studied in dimethyl sulfoxide (DMSO) solvent. The catalytic activity of the Cu complex increases in the following order; Cu-(styrene-vinylpyridine copolymer) (St·VP) complex > Cu-partially quarternized (by benzyl chloride) poly(vinylpyridine)(BCQP) complex > Cu-poly(vinylpyridine) (PVP) complex > Cu-pyridine (Py) complex > Cu-partially quarternized (by ethyl bromide) poly(vinylpyridine) (EBQP) complex. This order is the same as that of the reoxidation rate constant of the catalyst. Acceleration of ko process in Cu-St>VP and Cu-BCQP systems, where the active site is in the nonpolar field formed by the polymer ligand, is explained by an increase in strength of the coordination bonds.

12 citations

Patent
25 Aug 1975
TL;DR: In this article, 2,6-xylenol is methylated to yield 2,3,6 trimethylphenol in high selectivity in a liquid phase reaction controlled in temperature, pressure, and reactor residence time.
Abstract: 2,6-xylenol is methylated to yield 2,3,6-trimethylphenol in high selectivity in a liquid phase reaction controlled in temperature, pressure, and reactor residence time.

11 citations

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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20211
20152
20111
20101
20092
20021