Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2179876Erstellt: 24. Oktober 2026

Ethanol → 2-(2-Methylpentylthio)-1,3,4-thiadiazole-5-amine

https://huagongshe.com/de/reaction/2179876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium HydroxideHCID 14798—
Edukt2-Methyl-1-pentyl methanesulfonateHCID 22486761—
EduktHCID 178509208HCID 178509208—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2-Methylpentylthio)-1,3,4-thiadiazole-5-amineHCID 22486760—

Reaktionsschritte

A three-necked 3-L round bottom flask was charged with 2-methylpentyl methanesulphonate (90 g, 0.5 mol), ethanol (1.5 L) and 2-mercapto-1,3,4-thiadiazole-5-amine (66.5 g, 0.5 mol). Sodium hydroxide (20 g, 0.5 mol) was added to the stirred suspension. The mixture was heated to reflux and held at reflux over night. As the mixture warmed the cream suspension gradually dissolved. Just before refluxing began a cloudy precipitate formed. The reaction mixture was cooled to room temperature, filtered, and the residue was washed well with ethanol. The resulting filtrate was concentrated to dryness to give an off-white solid that was dissolved in ethyl acetate (1.2 L) and washed with 1) water (800 mL) and 2) brine (1 L). The filtrate was dried (MgSO4) and concentrated to dryness. An off-white solid was obtained that was recrystallised from boiling acetonitrile (150 mL). The filtered material was washed well with acetonitrile and dried (Vac/40° C.). The required product was obtained as a white solid wt 83 g; 76.5%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06887656B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-35b097b0764b4dc9a89fcac955e74450
Quellennotizuspto-grants-2005_05