Journal2012

Triethylamine-bonded sulfonic acid ([Et3N–SO3H]Cl): a highly efficient and homogeneous catalyst for the condensation of 2-naphthol with arylaldehydes and amides (alkyl carbamates or thioamides)

Abdolkarim Zare, Shayesteh Akbarzadeh, Elmira Foroozani, Hamideh Kaveh, Ahmad Reza Moosavi‐Zare, Alireza Hasaninejad, Mohammad Mokhlesi, Mohammad Hassan Beyzavi, Mohammad Ali Zolfigol

Journal of Sulfur Chemistry Vol. 33, No. 3, 259–272

چکیده

Ionic liquid triethylamine-bonded sulfonic acid ([Et 3N–SO 3H]Cl, N,N-diethyl-N-sulfoethanammonium chloride) is utilized as a highly efficient, inexpensive and homogeneous catalyst to promote the following one-pot multi-component organic transformations under solvent-free conditions: (i) the condensation of 2-naphthol with arylaldehydes and amides leading to 1-amidoalkyl-2-naphthols, (ii) the reaction of 2-naphthol with aromatic aldehydes and alkyl carbamates to produce 1-carbamatoalkyl-2-naphthols, and (iii) the condensation between 2-naphthol, arylaldehydes and thioamides leading to 1-thioamidoalkyl-2-naphthols. High yields, short reaction times, efficiency, generality, clean process, simple methodology, low cost, easy work-up, ease of preparation of the catalyst, and environmentally benign conditions are some advantages of the protocols.

موضوعات و کلیدواژه‌ها

Multicomponent Synthesis of HeterocyclesChemical Synthesis and ReactionsSulfur-Based Synthesis TechniquesTriethylamineChemistryCatalysisAlkylCondensationIonic liquidCondensation reactionOrganic chemistrySulfonic acidHomogeneousSolventHomogeneous catalysis

ارجاع علمی

Abdolkarim Zare, Shayesteh Akbarzadeh, Elmira Foroozani, Hamideh Kaveh, Ahmad Reza Moosavi‐Zare, Alireza Hasaninejad, Mohammad Mokhlesi, Mohammad Hassan Beyzavi, Mohammad Ali Zolfigol. “Triethylamine-bonded sulfonic acid ([Et3N–SO3H]Cl): a highly efficient and homogeneous catalyst for the condensation of 2-naphthol with arylaldehydes and amides (alkyl carbamates or thioamides).” Journal of Sulfur Chemistry, 2012. https://doi.org/10.1080/17415993.2012.690415