Synthesis of Aromatic Aldehydes by CH Formylation of Aromatics with Silyl Formates Prepared from CO <sub>2</sub> and Hydrosilanes
Despite the recent remarkable progress in CO 2 fixation reactions, the methods for the synthesis of aldehydes from CO 2 are quite limited partly because of the lability of the resulting formyl group and difficulty in the controlled deoxygenative CO 2 conversions leading to CH and CC bond formation. Here, we have developed the direct CH formylation of electron‐rich aromatics using silyl formates, prepared from CO 2 and hydrosilanes, in the presence of BCl 3 or BBr 3 . This is the first report on the direct CH formylation of aromatics with silyl formates. Useful compounds including a biologically active compound and octaethylporphyrin were synthesized by fixing one to four CO 2 molecules in a stepwise manner. DFT calculations have been done to elucidate the reaction mechanism including a dual role of BBr 3 in the activation of silyl formate, HCO 2 SiMe 2 Ph, and electrophilic aromatic substitution.
Authors
- Natsumi Nitta (ORCID: https://orcid.org/0009-0006-1588-041X)
- Kazuto Takaishi (ORCID: https://orcid.org/0000-0003-4979-7375)
- Bikash Dev Nath (ORCID: https://orcid.org/0009-0002-9585-5185)
- Tadashi Ema (ORCID: https://orcid.org/0000-0002-2160-6840)
- So Saibara
- Kei Hirokawa
Institutions
- Okayama University of Science (JP)
- Okayama University (JP)
- Dhaka University of Engineering & Technology (BD)
- Islamic University of Technology (BD)
Publication Details
- Journal
- Advanced Synthesis & Catalysis
- Published
- 2026-06-09
- DOI
- https://doi.org/10.1002/adsc.70571
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Okayama Foundation for Science and Technology