84547-96-6Relevant articles and documents
Hydrogen halides as nucleophilic agents for 3,4,5-trinitro-1H-pyrazoles
Dalinger, Igor L.,Vatsadze, Irina A.,Shkineva, Tatyana K.,Popova, Galina P.,Shevelev, Svyatoslav A.
, p. 43 - 44 (2012)
1-R-3,4,5-Trinitropyrazoles (R = H, Me) undergo nucleophilic substitution on treatment with concentrated hydrogen halide solutions to give 5-halo-1-R-3,4-dinitropyrazoles.
Efficient procedure for high-yield synthesis of 4-substituted 3,5-dinitropyrazoles using 4-chloro-3,5-dinitropyrazole
Dalinger, Igor L.,Vatsadze, Irina A.,Shkineva, Tatyana K.,Popova, Galina P.,Shevelev, Svyatoslav A.
experimental part, p. 2058 - 2064 (2012/08/07)
The transformations of readily available 4-chloro-3,5-dinitropyrazole and its N-methylated derivative under the action of anionic S-/O-nucleophiles and neutral N-nucleophiles were studied. Independent of the substrate's charge (anionic, R=H, or neutral, R
NITRATION OF 4-HALO-1-METHYLPYRAZOLES IN SULFURIC ACID
Perevalov, V. P.,Manaev, Yu. A.,Baryshnenkova, L. I.,Kanep, E. E.,Andreeva, M. A.,Stepanov, B. I.
, p. 1081 - 1083 (2007/10/02)
The rate of nitration of 4-bromo- and 4-chloro-1-metylpyrazoles with nitric acid in various concentrations of sulfuric acid is higher at position 5 than at position 3.