The regioselective nitration of 9,9′-spirobifluorene under mild conditions is reported for the first time by operating under Menke’s and Crivello’s conditions. The optimized protocol allows obtaining 2-nitro and 2,2′-dinitro-9,9′-spirobifluorene in yields of 79 and 95% and, for the first time, 2,2′,7-trinitro-9,9′-spirobifluorene with 66% yield. Besides, the role of dinitrate salt in Crivello’s protocol has been now clarified, which opens novel scenarios in the preparation of functional materials.

Regioselectivity Control in Spirobifluorene Nitration under Mild Conditions: Explaining the Crivello’s Reagent Mechanism / D. Yousif, L. Vaghi, C.G. Daniliuc, R. Po, A. Papagni, F. Rizzo. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - 88:9(2023 Apr 26), pp. 5285-5290. [10.1021/acs.joc.2c02596]

Regioselectivity Control in Spirobifluorene Nitration under Mild Conditions: Explaining the Crivello’s Reagent Mechanism

F. Rizzo
Ultimo
2023

Abstract

The regioselective nitration of 9,9′-spirobifluorene under mild conditions is reported for the first time by operating under Menke’s and Crivello’s conditions. The optimized protocol allows obtaining 2-nitro and 2,2′-dinitro-9,9′-spirobifluorene in yields of 79 and 95% and, for the first time, 2,2′,7-trinitro-9,9′-spirobifluorene with 66% yield. Besides, the role of dinitrate salt in Crivello’s protocol has been now clarified, which opens novel scenarios in the preparation of functional materials.
Settore CHIM/06 - Chimica Organica
26-apr-2023
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1094851
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