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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2067324Erstellt: 26. Oktober 2026

Cyanogen Bromide → HCID 178508456, Verbindung

https://huagongshe.com/reaction/2067324

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanogen BromideHCID 10476—
EduktSodium HydroxideHCID 14798—
EduktN-BenzylethylenediamineHCID 77801—
LösungsmittelEthanolHCID 702—
ProduktHCID 178508456HCID 17850845696%

Reaktionsschritte

To a solution of N-benzylethane-1,2-diamine (1.00 g, 6.65 mmol) in absolute ethanol (25 mL) was added cyanogen bromide (0.92 g, 8.65 mmol). The reaction mixture was stirred at ambient temperature for 1 hour, then cooled in an ice water bath. The pH of the solution was adjusted to ˜10 by the addition of 1 M sodium hydroxide solution dropwise. The solvent was concentrated in vacuo. The residue was diluted with ethyl acetate (100 mL), washed with water (200 mL) and brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the concentrated in vacuo. The residue was recrystallized in ethyl acetate and hexane to yield the title compound as a colorless solid in 96% yield (1.12 g): mp 165-167° C. (ethyl acetate/hexanes); 1H NMR (300 MHz, DMSO-d6) δ 7.39-7.24 (m, 6H), 4.47 (s, 2H), 3.49-3.33 (m, 4H); 13C NMR (75 MHz, DMSO-d6) δ 159.4, 136.0, 129.1, 128.2, 128.1, 48.1, 47.4, 41.3; MS (ES+) m/z 176.3 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08293768B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-ae298e0b948a4201a03f15288e211bc1
Quellennotizuspto-grants-2012_10