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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1649585Erstellt: 25. Oktober 2026

Methanol, (methylnitramino)- → Methanediamine, N,N'-dimethyl-N,N'-dinitro-

https://huagongshe.com/reaction/1649585

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanol, (methylnitramino)-HCID 119262—
EduktMethanamine, N-nitro-HCID 421670—
ProduktMethanediamine, N,N'-dimethyl-N,N'-dinitro-HCID 25794—

Reaktionsschritte

An additional mole of methylnitramine is reacted with the 2-nitro-2-aza-1-propanol to produce 2,4-dinitro-2,4-diazapentane. The reactants (in approximately a 1:1 molar ratio) are dissolved in a suitable organic solvent and the resulting solution is added to concentrated sulfuric acid at a controlled rate. The reaction temperature is maintained at a temperature above the freezing point of the concentrated sulfuric acid up to 5° C., but preferably from -5° C. to 0° C. The product 2,4-dinitro-2,4-diazapentane is then isolated by extraction using a suitable organic solvent, washing to remove traces of the acid, evaporating off the solvent, and then recrystallizing the resulting solid. A suitable organic solvent is one that (1) is capable of holding the methylnitramine and 2-nitro-2-aza-1-propanol starting materials and the 2,4-dinitro-2,4-diazapentane product in solution, (2) chemically inert to concentrated sulfuric acid, and (3) essentially immiscible with concentrated sulfuric acid. Suitable solvents include methylene chloride, chloroform, 1,2-dichloroethane, and 1,1,2-trichloroethane. Methylene chloride is the most preferred solvent.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04418212
Quelldatensatzuspto-grants-1983_11
ORD IDord-bca30cf26d234774ae87aed118c198a5
Quellennotizuspto-grants-1983_11