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CO2 -Based Carbamate Synthesis Utilizing Reusable Polymer-Supported DBU.
Mora Vargas, Jorge Andrés; Burtoloso, Antonio C B.
Afiliación
  • Mora Vargas JA; Institute of Chemistry of São Carlos, University of São Paulo, São Carlos, São Paulo, CEP, 13560-970, Brazil.
  • Burtoloso ACB; Institute of Chemistry of São Carlos, University of São Paulo, São Carlos, São Paulo, CEP, 13560-970, Brazil.
ChemSusChem ; 16(23): e202300936, 2023 Dec 07.
Article en En | MEDLINE | ID: mdl-37584441
The present study highlights a novel and advantageous protocol for accessing carbamates through the well-established three-component coupling reaction involving CO2 , amines, and alkyl halides. By employing an immobilized organic base, operating under mild reaction conditions, an array of alkyl carbamates in yields of up to 95 % could be isolated. This approach offers a broad and versatile product scope, allowing for the facile modification of both the amine and alkyl halide reactants. Notably, the pioneering use of an immobilized organic base, specifically the polymer-supported 1,8-diazabicyclo[5.4.0]undec-7-ene (PS-DBU), in this three-component reaction eliminates the need for classical purification steps, streamlining the process. To ensure practicality and sustainability, extensive studies were conducted to verify the recovery and reusability of the polymer-supported DBU catalyst, which consistently maintained the high chemical yield of the carbamates across multiple cycles. Overall, this innovative protocol represents a significant advancement in carbamate synthesis, combining efficiency, generality, and the potential for DBU recycling.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: ChemSusChem Asunto de la revista: QUIMICA / TOXICOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: ChemSusChem Asunto de la revista: QUIMICA / TOXICOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Alemania