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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2023 Volume 33, Issue 6, Pages 841–843 (Mi mendc543)

This article is cited in 3 papers

Communications

Ethyl butyrates bearing nitro and difluoroamino groups

I. L. Dalinger, T. K. Shkineva, A. B. Sheremetev

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Difluoroamination and esterification reactions were utilized for the preparation of NF2-analogs of 2,2,2-trinitroethyl 4,4,4-trinitrobutanoate with replacing one or two nitro groups. Difluoroamino products possess promising properties as ingredients of metallized energetic materials.

Keywords: difluoroamino group, difluoroamino(dinitro)methyl group, nitro alcohols, energetic alkyl esters, decomposition temperature, impact sensitivity.

Language: English

DOI: 10.1016/j.mencom.2023.10.034



© Steklov Math. Inst. of RAS, 2025