Herein, we report a simple and efficient protocol for the deprotection of acetate and benzoate to alcohols, catalyzed by an imidazolium-based acid. Acetate groups were selectively removed while benzoate groups remained intact under mild conditions, and benzoate needed harsher conditions. Notably, this protocol was successfully employed for carbohydrate-building block synthesis in a one-pot strategy, was compatible with different ester protecting groups such as O-Bz, O-Ts, and O-Piv and site-selective deprotection of acetate. The reusable, environmentally benign catalyst enabled smooth operation, resulting in a promising protocol for deprotection.
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Ho et al. (2025) studied this question.
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