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 CH and CC bond formation. Here, we have developed the direct CH 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 CH 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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis of Aromatic Aldehydes by CH Formylation of Aromatics with Silyl Formates Prepared from CO 2 and Hydrosilanes

Natsumi Nitta, Kazuto Takaishi, Bikash Dev Nath, Tadashi Ema et al.
Advanced Synthesis & Catalysis
Carbon dioxide utilization in catalysis
article

Synthesis of Aromatic Aldehydes by CH Formylation of Aromatics with Silyl Formates Prepared from CO 2 and Hydrosilanes

Natsumi Nitta, Kazuto Takaishi, Bikash Dev Nath, Tadashi Ema, So Saibara, Kei Hirokawa
article en

Abstract

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 CH and CC bond formation. Here, we have developed the direct CH 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 CH 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.

Advanced Synthesis & CatalysisVol. 368(12)
Okayama University of Science (JP), Okayama University (JP), Dhaka University of Engineering & Technology (BD), Islamic University of Technology (BD)
Okayama Foundation for Science and Technology
Clean water and sanitation
Openalex Percentile: Top 14%
Carbon dioxide utilization in catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.