A continuous-flow two-step process for the production of multifunctional intermediate compounds was performed with a combination of two column reactors packed with different organic immobilized catalysts. The first step of the reaction, nitroaldol condensation between aromatic aldehydes and nitromethane, is promoted by a silica gel-supported primary amine; the second step, Michael addition of β-dicarbonyl compounds to the nitrostyrenes obtained in the first step, is catalyzed by a silica gel-supported guanidine TBD. In both cases, the catalysts can be directly reused for several runs with no significant changes in activity.

Use of Immobilized Organic Base Catalysts for Continuous-Flow Fine Chemical Synthesis / Soldi, Laura; Ferstl, W; Loebbecke, S; Maggi, Raimondo; Malmassari, C; Sartori, Giovanni; Yada, S.. - In: JOURNAL OF CATALYSIS. - ISSN 0021-9517. - 258:(2008), pp. 289-295. [10.1016/j.jcat.2008.07.005]

Use of Immobilized Organic Base Catalysts for Continuous-Flow Fine Chemical Synthesis

SOLDI, Laura;MAGGI, Raimondo;SARTORI, Giovanni;
2008-01-01

Abstract

A continuous-flow two-step process for the production of multifunctional intermediate compounds was performed with a combination of two column reactors packed with different organic immobilized catalysts. The first step of the reaction, nitroaldol condensation between aromatic aldehydes and nitromethane, is promoted by a silica gel-supported primary amine; the second step, Michael addition of β-dicarbonyl compounds to the nitrostyrenes obtained in the first step, is catalyzed by a silica gel-supported guanidine TBD. In both cases, the catalysts can be directly reused for several runs with no significant changes in activity.
2008
Use of Immobilized Organic Base Catalysts for Continuous-Flow Fine Chemical Synthesis / Soldi, Laura; Ferstl, W; Loebbecke, S; Maggi, Raimondo; Malmassari, C; Sartori, Giovanni; Yada, S.. - In: JOURNAL OF CATALYSIS. - ISSN 0021-9517. - 258:(2008), pp. 289-295. [10.1016/j.jcat.2008.07.005]
File in questo prodotto:
File Dimensione Formato  
Paper 1.pdf

non disponibili

Tipologia: Documento in Post-print
Licenza: Creative commons
Dimensione 169.1 kB
Formato Adobe PDF
169.1 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

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/11381/1863608
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 42
  • ???jsp.display-item.citation.isi??? 43
social impact