Direct synthesis of 3-methylbenzofuran from phenol and acetone over halide cluster catalysts taking advantage of acidic and metallic properties

Chemical Engineering Journal

Volumn 161, Issue 3, 2010, Pages 384-387

  Nagashima, Sayoko ^a   Kamiguchi, Satoshi ^b   Ohguchi, Satoshi ^a,b   Chihara, Teiji ^a  

^a SAITAMA UNIVERSITY   (Japan)

^b INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

Author keywords

2 Isopropenylphenol; Benzofuran synthesis; Br nsted acid; Halide cluster; Hydroxo ligand; Phenol acetone condensation

Indexed keywords

ACETONE CONDENSATION; ACID HALIDES; AQUA LIGANDS; BENZOFURANS; CATALYTIC ACTIVITY; CO-ORDINATIVELY UNSATURATED; CYCLODEHYDROGENATION; DIRECT SYNTHESIS; HALIDE CLUSTERS; HYDROGEN CHLORIDE; HYDROXO LIGANDS; METAL ATOMS; METALLIC PROPERTIES; REACTION TEMPERATURE; TEMPERATURE RANGE; TUNGSTEN CLUSTER;

ACETONE; ACIDS; CHELATION; CHLORINE COMPOUNDS; CONDENSATION; DEHYDROGENATION; HELIUM; LIGANDS; MOLYBDENUM; NIOBIUM; PHENOLS; PLATINUM; SILICA; SILICA GEL; SILICON COMPOUNDS; SYNTHESIS (CHEMICAL); TANTALUM; TUNGSTEN;

PLATINUM COMPOUNDS;

EID: 77953706892     PISSN: 13858947     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cej.2009.08.002     Document Type: Article

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