Related Experiment Video
Updated: Sep 3, 2025

Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source
Published on: August 17, 2018
A practical concept for catalytic carbonylations using carbon dioxide
Rui Sang1, Yuya Hu1, Rauf Razzaq1
1Leibniz-Institut für Katalyse e.V., Albert-Einstein-Str. 29a, 18059, Rostock, Germany.
This study introduces a novel two-step process for utilizing carbon dioxide (CO2) and hydrogen (H2) as feedstocks. A new catalyst efficiently converts CO2 into carbon monoxide (CO) for subsequent carbonylation reactions, producing valuable chemicals.
Area of Science:
- Catalysis
- Green Chemistry
- Organic Synthesis
Background:
- Atmospheric carbon dioxide (CO2) rise is a primary driver of global warming.
- CO2 utilization is crucial for sustainable chemical manufacturing.
- CO2 as a C1 feedstock offers a pathway to valuable chemicals.
Purpose of the Study:
- To develop a two-step cascade process for catalytic carbonylation using CO2.
- To utilize CO2 and H2 as feedstocks for producing aldehydes, esters, and amides.
- To demonstrate a sustainable method for synthesizing organic building blocks.
Main Methods:
- A novel heterogeneous copper catalyst (10Cu@SiO2-PHM) was synthesized.
- The catalyst facilitated the reduction of CO2 with H2 to generate carbon monoxide (CO).
- In situ generated CO was used in subsequent hydroformylation, alkoxycarbonylation, and aminocarbonylation reactions.
Main Results:
- The 10Cu@SiO2-PHM catalyst showed high selectivity (≥98%) and 27% conversion in CO generation.
- Various aldehydes, (unsaturated) esters, and amides were synthesized with high yields and selectivities.
- Reactions proceeded efficiently at low temperatures and ambient pressure.
Conclusions:
- The developed two-step cascade process effectively utilizes CO2 as a C1 feedstock.
- This method offers a sustainable route for producing important organic compounds.
- The approach is suitable for continuous synthesis in drug discovery and organic synthesis.
Related Concept Videos
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Loss of Carboxy Group as CO2: Decarboxylation of β-Ketoacids
Catalysis
Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

