TY - JOUR
T1 - Telescoped continuous flow synthesis of phenyl acrylamide
AU - Salaklang, Jatuporn
AU - Mertens, Erika
AU - Maes, Veronique
AU - Dams, Rudy
AU - Dermaut, Wim
AU - Junkers, Tanja
PY - 2020/8/27
Y1 - 2020/8/27
N2 - Functional acrylamides are valuable intermediates for organic synthesis and building blocks in many industrial areas, like polymer synthesis, fine chemicals and pharmaceutics. The conventional batch reaction copes with some safety issues, due to the intrinsic reactivity and careful handling of the reagents. Moreover, the hazardous solvents used and the energy consumed have an enormous environmental impact. The development of an efficient and robust continuous flow process, allowing a safe and on-demand synthesis of acrylamides with high yield leads the way to a more sustainable chemistry. Two alternative synthesis routes for the preparation of N-phenyl acrylamide, but applicable as a continuous production process, are presented: both based on the Schotten-Baumann reaction, one starting from 3-chloropropanoyl chloride and the other starting from acrylic acid. The latter reaction, with a laboratory throughput of 16.5 g·h−1, low operation temperatures and the use of less hazardous chemicals, provides an efficient and sustainable alternative synthesis route of the desired acrylamides, minimizing side-products and enabling a safe and convenient scale-up.
AB - Functional acrylamides are valuable intermediates for organic synthesis and building blocks in many industrial areas, like polymer synthesis, fine chemicals and pharmaceutics. The conventional batch reaction copes with some safety issues, due to the intrinsic reactivity and careful handling of the reagents. Moreover, the hazardous solvents used and the energy consumed have an enormous environmental impact. The development of an efficient and robust continuous flow process, allowing a safe and on-demand synthesis of acrylamides with high yield leads the way to a more sustainable chemistry. Two alternative synthesis routes for the preparation of N-phenyl acrylamide, but applicable as a continuous production process, are presented: both based on the Schotten-Baumann reaction, one starting from 3-chloropropanoyl chloride and the other starting from acrylic acid. The latter reaction, with a laboratory throughput of 16.5 g·h−1, low operation temperatures and the use of less hazardous chemicals, provides an efficient and sustainable alternative synthesis route of the desired acrylamides, minimizing side-products and enabling a safe and convenient scale-up.
KW - Acid chloride
KW - Acrylamide
KW - Flow chemistry
KW - Microreactor
UR - http://www.scopus.com/inward/record.url?scp=85089972246&partnerID=8YFLogxK
U2 - 10.1007/s41981-020-00113-6
DO - 10.1007/s41981-020-00113-6
M3 - Article
AN - SCOPUS:85089972246
VL - 10
SP - 673
EP - 679
JO - Journal of Flow Chemistry
JF - Journal of Flow Chemistry
SN - 2062-249X
IS - 4
ER -