Preparation and spectral properties of products of the reaction of N,N-dimethylhydrazine with selected enolethers/alkoxymethylene systems
Denisa Tarabová *, Viktor Milata †
Faculty of Chemical and Food Technology, Department of Organic Chemistry, Slovak University of Technology, Radlinského 9, SK-812 37 Bratislava, Slovak Republic
E-mail: * denisa.tarabova@stuba.sk, † viktor.milata@stuba.sk
Abstract: There were studied series of activated enolethers (alkoxymethylene derivatives of malonic or 3-oxobutanoic acids derivatives of general formula R—O—CH=C(R1, R2) where R1 = R2/ R1 ≠ R2 (R1, R2 = CO2CH3, CO2CH2CH3, COCH3, CN) with N,N-dimethylhydrazine. They smoothly provided products of nucleophilic vinylic substitution reaction — dimethyl hydrazinyl methylene derivatives of malonic or 3-oxobutanoic acids (enhydrazines), respectively from 20 minutes to 2 hours at room temperature.
Keywords: N,N-dimethylhydrazine, enolethers, nucleophilic vinylic substitution reaction, enhydrazines
Full paper in Portable Document Format: acs_0135.pdf
Acta Chimica Slovaca, Vol. 5, No. 2, 2012, pp. 232—235