Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374191Erstellt: 25. Oktober 2026

Ethanol, 2-amino-, 1-nitrate, nitrate (1:1) → N-cyano-N'-(2-nitroxyethyl)-3-furancarboximidamide

https://huagongshe.com/reaction/374191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanol, 2-amino-, 1-nitrate, nitrate (1:1)HCID 78397—
EduktSodium MethoxideHCID 10942334—
EduktMethyl N-cyano-3-furancarboximidateHCID 19734520—
LösungsmittelMethanolHCID 887—
ProduktN-cyano-N'-(2-nitroxyethyl)-3-furancarboximidamideHCID 197542508,2%

Reaktionsschritte

Methyl N-cyano-3-furancarboximidate (0.5 g, 3.3 mmol) was dissolved in methanol (10 ml), and 2 nitroxyethylamine nitrate (0.84 g, 5.0 mmol) and sodium methoxide (0.27 g, 5.0 mmol) were added. The mixture was stirred at room temperature for 26 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and the residue thus obtained was extracted with chloroform (60 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C 200, 20 g) eluting with chloroform-methanol (100:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.06 g, 0.27 mmol, yield: 8%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166347
Quelldatensatzuspto-grants-1992_11
ORD IDord-72ee8c912729413a94d38a7e76dc96e3
Quellennotizuspto-grants-1992_11