Ambient Pressure Hydroformylation – A Key Step to <i>Meso</i>‐Alkyl BODIPYs

Abstract Herein, a highly efficient five‐step reaction sequence to meso‐alkyl BODIPYs is presented. In our previous work, the hydroformylation of terminal alkenes was used to generate an aldehyde from an alkene via rhodium catalysis and use them in a subsequent tandem reaction to obtain BODIPY dyes. However, the use of higher pressures and therefore autoclaves as well as their necessary equipment might limit others to use this method. The refined approach in this work employs ambient pressure hydroformylation, done in a simple Schlenk tube and using a CO/H 2 balloon, as key step towards an easier meso‐alkyl BODIPY synthesis. Additionally, the use of MTBE instead of chloroform as reaction solvent results in a greener approach. Readily available and easily synthesizable alkenes as well as different pyrrole building blocks can be used to extend the range of known alkyl‐BODIPYs. The synthesis of 23 derivatives with overall yields of up to 67 % demonstrates the wide applicability and advantages of the refined method.

Authors

Institutions

Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-23
DOI
https://doi.org/10.1002/ejoc.202401089
Citations
1
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.12

Funders

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

Ambient Pressure Hydroformylation – A Key Step to Meso‐Alkyl BODIPYs

Felix Bauer, Bernhard Breit, L. L. MILLER
1 citations
European Journal of Organic Chemistry
Luminescence and Fluorescent Materials
0.12
article

Ambient Pressure Hydroformylation – A Key Step to Meso‐Alkyl BODIPYs

Felix Bauer, Bernhard Breit, L. L. MILLER
article en
1 citations

Abstract

Abstract Herein, a highly efficient five‐step reaction sequence to meso‐alkyl BODIPYs is presented. In our previous work, the hydroformylation of terminal alkenes was used to generate an aldehyde from an alkene via rhodium catalysis and use them in a subsequent tandem reaction to obtain BODIPY dyes. However, the use of higher pressures and therefore autoclaves as well as their necessary equipment might limit others to use this method. The refined approach in this work employs ambient pressure hydroformylation, done in a simple Schlenk tube and using a CO/H 2 balloon, as key step towards an easier meso‐alkyl BODIPY synthesis. Additionally, the use of MTBE instead of chloroform as reaction solvent results in a greener approach. Readily available and easily synthesizable alkenes as well as different pyrrole building blocks can be used to extend the range of known alkyl‐BODIPYs. The synthesis of 23 derivatives with overall yields of up to 67 % demonstrates the wide applicability and advantages of the refined method.

European Journal of Organic ChemistryVol. 28(3)
University of Freiburg (DE)
Fonds der Chemischen Industrie
Openalex Percentile: Top 59%
Luminescence and Fluorescent Materials
0.12
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.