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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720727Erstellt: 25. Oktober 2026

Water → 5-(4-bromo-phenyl)-3-methyl-1-(4-methylsulfanyl-phenyl)-1H-[1,2,4]triazole

https://huagongshe.com/reaction/720727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
Edukt(4-(Methylsulfanyl)phenyl)hydrazine hydrochlorideHCID 2760977—
EduktN-(1-ethoxy-ethylidene)-4-bromo-benzamideHCID 21894671—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(4-bromo-phenyl)-3-methyl-1-(4-methylsulfanyl-phenyl)-1H-[1,2,4]triazoleHCID 2189468366.005,5%

Reaktionsschritte

N-(1-ethoxy-ethylidene)-4-bromo benzamide 565 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and (4-methylsulfanyl-phenyl)-hydrazine hydrochloride 439 mg (2.23 mmol) was added to the solution. Then, triethylamine 0.35 ml (2.51 mmol) was slowly added dropwise at room temperature for 10 minutes and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was purified through a flash column chromatography (ethyl acetate:normal hexane=1:1). As a result, 5-(4-bromo-phenyl)-3-methyl-1-(4-methylsulfanyl-phenyl)-1H-[1,2,4]triazole (497 g, yield: 66%) was obtained as a liquid phase.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135572B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-7b6232892ca24f6887edc3731b54d9ce
Quellennotizuspto-grants-2006_11