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.
Authors
- Amanda Pecora
- Christopher W. am Ende (ORCID: https://orcid.org/0000-0001-8832-9641)
- John M. Humphrey (ORCID: https://orcid.org/0000-0001-8753-9479)
- Eddie X. Yang
- Ethan L. Fisher (ORCID: https://orcid.org/0000-0002-8700-5108)
Institutions
- Pfizer (United States) (US)
Publication Details
- 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
- Field-Weighted Citation Impact
- 0.00