The palladium-phenanthroline catalyzed carbonylation reaction of nitrobenzene to methyl phenylcarbamate is known to be accelerated by both the addition of aniline and a carboxylic acid. Here, we report that combining the acidic and amino function in the same molecule, 2-NH2C6H4COOH, anthranilic acid, an higher activity is observed with respect to the use of simple benzoic acid. The 4-amino isomer does not show the same increased activity.

Carbonylation of nitrobenzene to N-methyl phenylcarbamate catalyzed by palladium-phenanthroline complexes - Bifunctional activation by anthranilic acid / M. Gasperini, F. Ragaini, S. Cenini, E. Gallo. - In: JOURNAL OF MOLECULAR CATALYSIS. A: CHEMICAL. - ISSN 1381-1169. - 204(2003), pp. 107-114.

Carbonylation of nitrobenzene to N-methyl phenylcarbamate catalyzed by palladium-phenanthroline complexes - Bifunctional activation by anthranilic acid

M. Gasperini
Primo
;
F. Ragaini
Secondo
;
S. Cenini
Penultimo
;
E. Gallo
Ultimo
2003

Abstract

The palladium-phenanthroline catalyzed carbonylation reaction of nitrobenzene to methyl phenylcarbamate is known to be accelerated by both the addition of aniline and a carboxylic acid. Here, we report that combining the acidic and amino function in the same molecule, 2-NH2C6H4COOH, anthranilic acid, an higher activity is observed with respect to the use of simple benzoic acid. The 4-amino isomer does not show the same increased activity.
nitrobenzene; carbonylation; palladium; urethanes; carboxylic acids
Settore CHIM/03 - Chimica Generale e Inorganica
2003
Article (author)
File in questo prodotto:
File Dimensione Formato  
26) Pd_AcAntranil.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 108.9 kB
Formato Adobe PDF
108.9 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/185763
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 36
  • ???jsp.display-item.citation.isi??? 32
social impact