HEROVÁ, Dana and Pavel PAZDERA. Efficient solid support catalyzed mono-aza-Michael addition reactions of piperazine. Monatshefte für Chemie - Chemical Monthly. 2015, vol. 146, No 4, p. 653-661. ISSN 0026-9247. Available from: https://dx.doi.org/10.1007/s00706-014-1379-2.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Efficient solid support catalyzed mono-aza-Michael addition reactions of piperazine
Authors HEROVÁ, Dana (203 Czech Republic, belonging to the institution) and Pavel PAZDERA (203 Czech Republic, guarantor, belonging to the institution).
Edition Monatshefte für Chemie - Chemical Monthly, 2015, 0026-9247.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10401 Organic chemistry
Country of publisher Austria
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.131
RIV identification code RIV/00216224:14310/15:00081733
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1007/s00706-014-1379-2
UT WoS 000351279800015
Keywords in English Aza-Michael addition; Catalysis; Metal catalysis; One-pot synthesis; Resin-supported metal ion
Tags AKR, rivok
Changed by Changed by: Ing. Andrea Mikešková, učo 137293. Changed: 28/4/2015 09:35.
Abstract
We report new methods for the efficient mono-aza-Michael additions of piperazine to compounds with activated multiple carbon–carbon bond (functional derivatives of acrylic, propiolic, and acetylenedicarboxylic acid). This method is based on the reaction of piperazine-1-ium cation with alkenes or alkynes substituted by EWGs under catalysis by various metal ions supported on weakly acidic cation-exchanger resin. Starting piperazine-1-ium cation is generated in situ in methanol solution by mixing of piperazine and piperazine-1,4-diium dichloride in various ratios. It was found that solid support metal catalysis afforded target products in very good yields in shortened reaction times. A new method of N-monosubstituted piperazine derivative preparation is very beneficial, because until now no one has come up with the idea to use for protection of the one nitrogen atom of the piperazine its simple protonation. Computer modeling of behavior of piperazine depending on the pH was carried out and according to the results, we concluded that the protonation of the nitrogen atom is the simplest, most effective, and most elegant method of preventing unwanted formation of 1,4-disubstituted product. Assumption was fully confirmed by number of syntheses. The main advantages of our syntheses are great simplicity, one-pot performance, use of non-toxic solvents only, mild reaction conditions, no generation of waste, short time of reactions, and high yields.
Links
2A-1TP1/090, research and development projectName: Nové katalyzátory a činidla pro udržitelné zelené syntézy a kombinatoriální syntézy.
Investor: Ministry of Industry and Trade of the CR, New catalysts and reagents for sustainable green syntheses and combinatorial syntheses
PrintDisplayed: 25/7/2024 22:27