Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal
- Francesca Tentori*a
- Elisabetta Brenna*a
- Chiara Ferraria
- Francesco G. Gattia
- Maria Chiara Ghezzia
- Fabio Parmeggiania
- aDipartimento di Chimica, Materiali ed Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, Piazza Leonardo da Vinci 32, 20133, Milano, Italy.Read the publication that featured this abstract
Piperonal is a key ingredient of flavour and fragrance industry and a useful intermediate for the synthesis of fine chemicals. It is currently prepared by either ozonolysis or chromic acid oxidation of isosafrole, obtained upon isomerization of naturally abundant safrole. A chemo-enzymatic three-step procedure for the conversion of isosafrole into piperonal is herein described. Lipase-mediated perhydrolysis of EtOAc in the presence of H2O2 is employed to generate peracetic acid in situ and promote the epoxidation of isosafrole. The reaction mixture is submitted to methanolic KOH treatment to recover the corresponding mixture of vicinal diols. The latter is efficiently oxidized to piperonal using MnO2, periodically regenerated at the expense of tert-butylhydroperoxide (TBHP), which represents the terminal oxidant of this transformation. The use of continuous-flow conditions using a continuously-stirred tank reactor for the epoxidation, and a packed bed reactor for the final oxidation improves the productivity and stability of the whole method, with space-time yields of 75 mmol·g–1·h–1 and 120 mmol·g–1·h–1 , calculated as amount of generated product per catalyst amount per time.
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