Sulfonic Acid Promoted N -Boc-, N -Cbz-, and N -PMB Cleavage in 1,1,1,3,3,3-Hexafluoro-2-Propanol (HFIP) and Application to Acid Sensitive Substrates

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Authors: Eddie X. Yang, Amanda Pecora, Ethan L. Fisher, Christopher W. am Ende, John M. Humphrey
Cited by: 1
References: 19

Abstract

We report on the mild, sulfonic acid promoted removal of N -Boc, N -Cbz, and N -PMB protecting groups in 1,1,1,3,3,3-hexafluoro-2-propanol (hexafluoroisopropanol; HFIP). According to this method, the typical N -Boc group is removed within 5 min upon treatment with 1.0–1.1 mol equiv of a sulfonic acid, such as methanesulfonic acid in neat HFIP, or within 30 min when HFIP is used as a 10% additive in toluene or dichloromethane. The N -Cbz group is efficiently cleaved with 1.1 mol equiv of methanesulfonic acid in neat HFIP at a slower rate, with near-quantitative removal from typical substrates generally realized within 24 h at room temperature or in shorter durations with mild heating. When conducted accordingly, the acid is essentially consumed by the end of the reaction to afford a near-neutral pH solution. The N -PMB group is cleaved in high yield on treatment with ∼2 mol equiv of methanesulfonic acid in HFIP within a couple of hours at room temperature. The relative reaction rates for these processes allow for selective N -Boc cleavage over N -Cbz groups, affording the chemist orthogonal protection options despite each group being removable under similar acidic conditions.

Fields of Study & Subjects

Sulfur-Based Synthesis Techniques Chemical Synthesis and Reactions Chemical Synthesis and Analysis

Publication details

Journal / source
The Journal of Organic Chemistry
Publisher
American Chemical Society (ACS)
Volume
91
Issue
21
Pages
7126–7133
Publication date
18 May 2026
Language
EN