Authors
Piers St Onge, Brandon White, Han Yao, Travis Dudding, Stephen G Newman
Published in
Angewandte Chemie (International ed. in English). Pages e7132408. Aug 23, 2026. Epub Aug 23, 2026.
Abstract
The direct deprotonation of weakly acidic C(sp3)─H bonds remains a fundamental strategy for generating carbon nucleophiles, but typically requires strong bases, cryogenic conditions, and stepwise protocols. A general method enabling single-step deprotonation and alkylation of these substrates remains elusive. Herein, we report that a combination of 1,1,3,3-tetramethyldisiloxane (TMDSO) and potassium tert-butoxide (KOtBu) enables the direct alkylation of weakly acidic substrates, particularly 2-alkyl and 4-alkyl pyridines, in a single operational step using simple alkyl halide electrophiles. A broad range of C─H alkylation products is obtained via in situ activation and alkylation, without the need for preformation of organometallic intermediates. Mechanistic experiments and DFT calculations support a pathway in which TMDSO and KOtBu cooperatively generate a transient, substrate-associated hydridic base with KH-like reactivity. Key substrate-potassium interactions, including N-coordination and cation-π binding, preorganize the system and enable rate-determining deprotonation with concurrent H2 evolution, followed by SN2 alkylation. These findings reveal a distinct mode of base activation that combines high basicity with unusual tolerance of alkyl halides, providing a practical approach to the alkylation of weakly acidic C─H bonds.
PMID:
42633667
Bibliographic data and abstract were imported from PubMed on 24 Aug 2026.
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