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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720727Generated: October 25, 2026

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

https://huagongshe.com/reaction/720727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant(4-(Methylsulfanyl)phenyl)hydrazine hydrochlorideHCID 2760977—
ReactantN-(1-ethoxy-ethylidene)-4-bromo-benzamideHCID 21894671—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-(4-bromo-phenyl)-3-methyl-1-(4-methylsulfanyl-phenyl)-1H-[1,2,4]triazoleHCID 2189468366,005.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135572B2
Source datasetuspto-grants-2006_11
ORD IDord-7b6232892ca24f6887edc3731b54d9ce
Source noteuspto-grants-2006_11