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

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.

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Journal
The Journal of Organic Chemistry
Published
2026-05-18
DOI
https://doi.org/10.1021/acs.joc.5c02406
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

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

Amanda Pecora, Christopher W. am Ende, John M. Humphrey, Eddie X. Yang et al.
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

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

Amanda Pecora, Christopher W. am Ende, John M. Humphrey, Eddie X. Yang, Ethan L. Fisher
article en

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.

The Journal of Organic Chemistry
Pfizer (United States) (US)
Clean water and sanitation
Openalex Percentile: Top 10%
Sulfur-Based Synthesis Techniques
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