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Hydrothermal alkylation of phenols with alcohols in diluted acids

Smutek, Bernhard, Kunz, Werner and Goettmann, Frederic (2012) Hydrothermal alkylation of phenols with alcohols in diluted acids. Comptes Rendus Chimie 15 (1), pp. 96-101.

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Abstract

Diluted acids (typically 0.05 M HCl) are shown to be very effective media to promote the alkylation of phenols with activated alcohols under hydrothermal conditions (from 150 to 200 °C). These results are an elegant alternative to “usual” Friedel-Crafts alkylations avoiding the use of alkylchlorides as alkylating agents and the use of Lewis acidic promoters or concentrated acids but also shade some light on the processes occurring during the hydrothermal carbonisation (HTC) of biomass.


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Item type:Article
Date:2012
Institutions:Chemistry and Pharmacy > Institut für Physikalische und Theoretische Chemie > Chair of Chemistry VI - Physical Chemistry (Solution Chemistry) > Prof. Dr. Werner Kunz
Identification Number:
ValueType
10.1016/j.crci.2011.11.016DOI
CODEN:CRCOCROther
CAN156:202817Other
Keywords:Hydrothermal synthesis; Diluted acid; Friedel-Crafts; Phenol; Benzyl alcohol
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:24261
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