Abstract
An efficient, scalable and sustainable method for the quantitative deprotection of thetert-butyl carbamate (N-Boc) protecting group is described, using down to near-stoichiometric amounts of hydrogen chloride gas in solvent-free conditions. We demonstrate theex situgeneration of hydrogen chloride gas from sodium chloride and sulfuric acid in a two-chamber reactor, introducing a straightforward method for controlled and stoichiometric release of HCl gas. The solvent-free conditions allow deprotection of a wide variety ofN-Boc derivatives to obtain the hydrochloride salts in quantitative yields. The procedure obviates the need for any work-up or purification steps providing an uncomplicated green alternative to standard methods. Due to the solvent-free, anhydrous conditions, this method shows high tolerance towards acid sensitive functional groups and furnishes expanded functional group orthogonality.
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CITATION STYLE
Verschueren, R. H., Gilles, P., Van Mileghem, S., & De Borggraeve, W. M. (2021). Solvent-freeN-Boc deprotection byex situgeneration of hydrogen chloride gas. Organic and Biomolecular Chemistry, 19(26), 5782–5787. https://doi.org/10.1039/d1ob00728a
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