α-C(sp <sup>3</sup> )–H Acetalization of Cyclic and Aliphatic Ethers Mediated by <i>N</i> -Bromoamides
High Resolution Image Download MS PowerPoint Slide A facile and catalyst-free method for the α-C(sp 3 )–H acetalization of cyclic and aliphatic ethers mediated by N -bromoamide DBDMH is reported. The reaction proceeds under mild conditions and exhibits a broad substrate scope. Common ethers, such as THF and Et 2 O, as well as a variety of functionalized alcohols, were efficiently transformed, affording the corresponding acetals in high yields. The developed protocol was further applied to the synthesis of the fragrances Cyanophyll and Efetaal, highlighting its practical utility. Mechanistic studies indicate that the impurities in commercial DBDMH such as molecular bromine and acids were crucial for the high reaction efficiency.
Authors
- Ying‐Yeung Yeung (ORCID: https://orcid.org/0000-0001-9881-5758)
- Qingyu Zhang
- Yat-Long Cheng
Institutions
- Chinese University of Hong Kong (HK)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-06-24
- DOI
- https://doi.org/10.1021/acs.orglett.6c02125
- Primary Topic
- Vanadium and Halogenation Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Research Grants Council, University Grants Committee
- Innovation and Technology Commission
- Chinese University of Hong Kong
- National Science Fund for Distinguished Young Scholars