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

Author:

Pollon Davide1,Annunziata Francesca23ORCID,Paganelli Stefano14ORCID,Tamborini Lucia2ORCID,Pinto Andrea3ORCID,Fabris Sabrina1,Baldo Maria Antonietta1ORCID,Piccolo Oreste5ORCID

Affiliation:

1. Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca’ Foscari Venezia, Via Torino 155, Venezia Mestre, 30170 Venezia, Italy

2. Dipartimento di Scienze Farmaceutiche, Università degli Studi di Milano, Via Mangiagalli 25, 20133 Milano, Italy

3. Dipartimento di Scienze per gli Alimenti, la Nutrizione e l’Ambiente, Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy

4. Consorzio Interuniversitario Reattività Chimica e Catalisi (CIRCC), Via Celso Ulpiani 27, 70126 Bari, Italy

5. Studio di Consulenza Scientifica SCSOP, Via Bornò 5, 23896 Sirtori, Italy

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.

Funder

institutional funding of Ca’ Foscari University Venice

Publisher

MDPI AG

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