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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1107886Erstellt: 26. Oktober 2026

Cyanogen Bromide → 5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/1107886

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanogen BromideHCID 10476—
Edukt2-NaphthohydrazideHCID 123485—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amineHCID 1870747620%

Reaktionsschritte

To a stirred solution of naphthalene-2-carboxylic acid hydrazide (0.6 g, 3.22 mmol, prepared as described in example 1) in dioxane (20 ml) was added a solution of sodium hydrogen carbonate (0.27 g, 3.22 mmol) in water (15 ml) and the resulting mixture was stirred for 5 min. To the reaction mixture was added cyanogen bromide (0.35 g, 3.3 mmol) and the mixture was stirred for 3 h at room temperature. The precipitate was filtered off and washed with diethyl ether (2×15 ml) and dried in vacuo at 50° C. affording 0.4 g of crude product which was suspended in absolute ethanol (15 ml) and stirred at reflux temperature for 0.5 h. The cooled suspension was filtered and the filter cake was dried in vacuo at 50° C. affording 130 mg (20%) of the title compound as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06063800
Quelldatensatzuspto-grants-2000_05
ORD IDord-0c05ee54ecef44baa159e5456f9e3a1c
Quellennotizuspto-grants-2000_05