An environmentally friendly synthesis of 2,4-dihydroxybenzophenone by the single-step O-mono-benzoylation of 1,3-dihydroxybenzene (resorcinol) and Fries rearrangement of intermediate resorcinol monobenzoate: The activity of acid-treated montmorillonite clay catalysts

Comptes Rendus Chimie

Volumn 7, Issue 2, 2004, Pages 143-150

  Bolognini, Marco ^a,b   Cavani, Fabrizio ^a,b   Cimini, Massimo ^b   Dal Pozzo, Luca ^b   Maselli, Luca ^a   Venerito, Donato ^b   Pizzoli, Fabio ^c   Veronesi, Giuseppe ^c  

^a INSTM   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c CIBA GEIGY LTD   (Switzerland)

Author keywords

2,4 dihydroxybenzophenone; Fries rearrangement; Liquid phase acylation; Montmorillonites; O Mono benzoylation; Resorcinol

Indexed keywords

BENZOIC ACID; BENZOPHENONE DERIVATIVE; CHLORIDE; MONTMORILLONITE; RESORCINOL; RESORCINOL DERIVATIVE; WATER;

ACIDITY; ACYLATION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL PROCEDURES; CHEMICAL REACTION; CONTROLLED STUDY; ENVIRONMENTAL PROTECTION; LIQUID; REACTION ANALYSIS; SYNTHESIS;

EID: 1842853962     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2003.12.005     Document Type: Article

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