Synthesis 1988; 1988(11): 893-894
DOI: 10.1055/s-1988-27742
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

A Simple Route to Racemic Acenaphthene-1-carboxylic Acid via Hydroformylation of Acenaphthylene

Andrea Raffaelli* , Carlo Rosini, Massimo Dini, Piero Salvadori
  • *Centro di Studio del C.N.R. per le Macromolecole Stereordinate ed Otticamente Attive, Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Via Risorgimento, 35, I-56126 Pisa, Italy
Further Information

Publication History

Publication Date:
20 August 2002 (online)

Hydroformylation of acenaphthylene using di-μ-chlorotetracarbonyl-dirhodium/triphenylphosphine as catalytic precursor affords acenaphthene-1-carboxaldehyde under mild conditions in 80% yield. This compound is easily transformed, via dehydration of the corresponding oxime followed by hydrolysis of the nitrile, into acenaphthene-1-carboxylic acid in an overall yield of ≍ 50%.

    >