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Brønsted Acid–Lewis Acid (BA–LA) Induced Final Deprotection/Peptide Resin Cleavage in Fmoc/<i>t-</i>Bu Solid-Phase Peptide Synthesis: HCl/FeCl<sub>3</sub> and AcOH/FeCl<sub>3</sub> as Viable PFAS-Free Alternatives for TFA

Jan Pawlas, Christophe André, Jon H. Rasmussen, Olivier Ludemann‐Hombourger

2024Organic Letters14 citationsDOI

Abstract

The widely used Fmoc/ t -Bu solid-phase peptide synthesis (SPPS) is hampered by relying on corrosive, per/polyfluoroalkyl substance (PFAS) classified trifluoroacetic acid (TFA) as a universal protecting group (PG) removal/resin cleavage reagent. We report that suitable combinations of Brønsted acids (BAs) and Lewis acids (LAs) such as HCl/FeCl 3 and AcOH/FeCl 3 constitute viable alternatives for TFA as PFAS-free cleavage agents. Using water miscible dimethyl carbonate (DMC) and acetonitrile (MeCN) as solvents enabled diluting cleavage mixtures with suitable aqueous solutions, allowing for direct use in purification in which removal of >99.99% iron from an HCl/FeCl 3 induced cleavage was demonstrated.

Topics & Concepts

ChemistryTrifluoroacetic acidCleavage (geology)ReagentAcetonitrileAqueous solutionPeptide synthesisBrønsted–Lowry acid–base theoryLewis acids and basesSolid-phase synthesisPeptideCombinatorial chemistryOrganic chemistryCatalysisFracture (geology)EngineeringGeotechnical engineeringBiochemistryChemical Synthesis and AnalysisChemical Synthesis and ReactionsFluorine in Organic Chemistry
Brønsted Acid–Lewis Acid (BA–LA) Induced Final Deprotection/Peptide Resin Cleavage in Fmoc/<i>t-</i>Bu Solid-Phase Peptide Synthesis: HCl/FeCl<sub>3</sub> and AcOH/FeCl<sub>3</sub> as Viable PFAS-Free Alternatives for TFA | Litcius