Friedel-Crafts Benzoylation of Anisole in Ionic Liquids: Catalysis, Separation, and Recycle Studies


Autoria(s): Hardacre, Christopher; Nancarrow, Paul; Rooney, David; Thompson, Jillian
Data(s)

21/11/2008

Resumo

The comparison of three ionic liquid-mediated catalytic processes for the benzoylation of anisole with benzoic anhydride is presented. A detailed understanding of the mechanism by which the zeolite and metal triflate reactions in bis{trifluoromethanesulfonyl}imide-based ionic liquids has been reported previously, and these routes are considered together with an indium chloride-based ionic liquid system. Solvent extraction and vacuum/steam distillation have been assessed as possible workup procedures, and an overall preliminary economic evaluation of each overall process is reported. Although the predominant activity is associated with the in situ formation of a homogeneous acid catalyst, the low cost and facile separation of the zeolite-catalysed process leads to this route being the most economically viable overall option. The results of a continuous flow miniplant based on the zeolite catalyst are also presented and compared with the reaction using a small plug How reactor.

Identificador

http://pure.qub.ac.uk/portal/en/publications/friedelcrafts-benzoylation-of-anisole-in-ionic-liquids-catalysis-separation-and-recycle-studies(e6e7c0c5-6f38-4820-8a64-717914aae0e2).html

http://dx.doi.org/10.1021/op800134k

http://www.scopus.com/inward/record.url?scp=58149123062&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Hardacre , C , Nancarrow , P , Rooney , D & Thompson , J 2008 , ' Friedel-Crafts Benzoylation of Anisole in Ionic Liquids: Catalysis, Separation, and Recycle Studies ' Organic Process Research & Development , vol 12 , no. 6 , pp. 1156-1163 . DOI: 10.1021/op800134k

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry #/dk/atira/pure/subjectarea/asjc/1600/1606 #Physical and Theoretical Chemistry
Tipo

article