Synthesizing o-bromobenzenethiols from aryne intermediates: This innovative method involves bromothiolation of aryne intermediates, resulting in the formation of highly functional o-bromobenzenethiols, which can be subsequently used to prepare diverse organosulfur compounds. (Source: Suguru Yoshida from Tokyo University of Science)
Unlocking Complex Sulfur Molecules

A Novel Approach for Synthesis of Functionalized Benzenethiol Equivalents

Organosulfur skeletons are crucial in many fields, including pharmaceuticals and electronics. Synthesizing organosulfur skeletons requires o-bromobenzenethiols. However, conventional methods face challenges due to quick oxidation and formation of highly reactive intermediates. In a new study, researchers from Japan developed a new method for synthesizing o-bromobenzenethiols from aryne intermediates via bromothiolation. This method can pave the way for the synthesis of new organosulfur compounds with applications in diverse fields.

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Kevin Anderson, Vice President Amines, Acetylene & Carbonyl Derivatives for North America, BASF (left) and Stefan Ali, Vice President, Energy Transition, Enerflex, in Houston, Texas (right) after signing the MOU at Enerflex’s office. (Source: BASF )
Decarbonization

Enerflex Partners with BASF for CCUS Applications

Under a MOU signed between Enerflex and BASF, both the firms will work together to facilitate the commercial scale deployment of carbon capture, utilization and storage (CCUS) applications. For this, the parties will combine Enerflex’s expertise in engineering, manufacturing, and integration of gas processing and compression systems with BASF’s proprietary Oase blue technology for flue gas and post-combustion CO2 capture.

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