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DOI: 10.1055/s-2006-942480
The HF/BF3-Catalysed Reaction of Substituted Benzenes with Carbon Monoxide
Publikationsverlauf
Publikationsdatum:
11. Juli 2006 (online)

Abstract
The HF/BF3-catalysed reactions of phenol and anisole as well as substituted benzenes with CO were investigated as possible routes to commercially important aldehydes.
The results confirmed that HF and BF3 are required in (at least) stoichiometric amounts for effective formylation with CO. With the aim of effecting truly catalytic reaction conditions, the formylation reactions were carried out in ionic liquids. It was shown that phenol is a good substrate for formylation in certain ionic liquids.
Key words
aldehydes - phenols - electrophilic aromatic substitutions - ionic liquids - Lewis acids
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Although care should be taken in the handling of the highly reactive alcohol 16, it could be prepared in almost quantitative yield via NaBH3 reduction of the corresponding ketone.
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