The acylation of 1,3-benzodioxole was studied in a continuous process using a recyclable heterogeneous substoichiometric catalyst. In a short time period (30 min), at 100 °C, the conversion rate was 73%, with a selectivity of 62% of the desired acylated product; the reaction was run continuously for 6 h, showing excellent stability and selectivity. Moreover, the unreacted starting material, 1,3-benzodioxole, can be easily separated by distillation and recycled.

Improved Process for the Continuous Acylation of 1,3-Benzodioxole / D. Pollon, F. Annunziata, S. Paganelli, L. Tamborini, A. Pinto, S. Fabris, M.A. Baldo, O. Piccolo. - In: MOLECULES. - ISSN 1420-3049. - 29:3(2024), pp. 726.1-726.10. [10.3390/molecules29030726]

Improved Process for the Continuous Acylation of 1,3-Benzodioxole

F. Annunziata
Secondo
;
L. Tamborini;A. Pinto;
2024

Abstract

The acylation of 1,3-benzodioxole was studied in a continuous process using a recyclable heterogeneous substoichiometric catalyst. In a short time period (30 min), at 100 °C, the conversion rate was 73%, with a selectivity of 62% of the desired acylated product; the reaction was run continuously for 6 h, showing excellent stability and selectivity. Moreover, the unreacted starting material, 1,3-benzodioxole, can be easily separated by distillation and recycled.
acylation of 1,3-benzodioxole; Brønsted or Lewis acids; flow chemistry; heterogeneous recyclable catalyst
Settore CHEM-05/A - Chimica organica
2024
Article (author)
File in questo prodotto:
File Dimensione Formato  
molecules-29-00726.pdf

accesso aperto

Descrizione: Article
Tipologia: Publisher's version/PDF
Dimensione 2.29 MB
Formato Adobe PDF
2.29 MB Adobe PDF Visualizza/Apri
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/2434/1101148
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact