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Sustainable Sulfonic Acid Functionalized Tubular Shape Mesoporous Silica as a Heterogeneous Catalyst for Selective Unsymmetrical Friedel-Crafts Alkylation in One Pot.
Singh, Sanjay; Kumar, Amit; Nebhani, Leena; Hazra, Chinmoy Kumar.
Affiliation
  • Singh S; Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
  • Kumar A; Department of Materials Science and Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
  • Nebhani L; Department of Materials Science and Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
  • Hazra CK; Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
JACS Au ; 3(12): 3400-3411, 2023 Dec 25.
Article in En | MEDLINE | ID: mdl-38155639
ABSTRACT
The development of general and more sustainable heterogeneous catalytic processes for Friedel-Crafts (FC) alkylation reactions is a key objective of interest for the synthesis of pharmaceuticals and commodity chemicals. Sustainable heterogeneous catalysis for the typical FC alkylation of an easily accessible carbonyl electrophile and arenes or with two different arene nucleophiles in one-pot is a prime challenge. Herein, we present a resolution to these issues through the design and utilization of a mesoporous silica catalyst that has been functionalized with sulfonic acid. For the synthesis of sulfonic acid-functionalized mesoporous silica (MSN-SO3H), thiol-functionalized mesoporous silica was first synthesized by the co-condensation method, followed by oxidation of the thiol functionality to the sulfonic acid group. Sulfonation of mesoporous silica was confirmed by 13C CP MAS NMR spectroscopy. Further, the devised heterogeneous catalysis using MSN-SO3H has been successfully employed in the construction of diverse polyalkanes including various bioactive molecules, viz arundine, tatarinoid-C, and late-stage functionalization of natural products like menthol and Eugenol. Further, we have utilized this sustainable technique to facilitate the formation of unsymmetrical C-S bonds in a one-pot fashion. In addition, the catalyst was successfully recovered and recycled for eight cycles, demonstrating the high sustainability and cost-effectiveness of this protocol for both academic and industrial applications.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JACS Au Year: 2023 Document type: Article Affiliation country: India Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JACS Au Year: 2023 Document type: Article Affiliation country: India Country of publication: United States