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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164376Generated: November 2, 2026

Triethylamine → 2-(4,5-Dichloro-imidazol-2-yl)-5-phenoxy-1,3,4-oxadiazole

https://huagongshe.com/reaction/1164376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydrazinecarboxylic acid, phenyl esterHCID 134791—
Reactant4,5-Dichloro-2-(trichloromethyl)-1H-imidazoleHCID 12482573—
Solvent1,4-DioxaneHCID 31275—
Product2-(4,5-Dichloro-imidazol-2-yl)-5-phenoxy-1,3,4-oxadiazoleHCID 13575544572.5%

Reaction Steps

16.7 g (0.11 mol) of carbazic acid phenyl ester were added in portions, at room temperature, to a solution of 25.4 g (0.1 mol) of 4,5-dichloro-2-trichloromethyl-imidazole in 200 ml of dioxane. After the slightly exothermic reaction had subsided, the mixture was gradually warmed to the boil and boiled for a further 2 hours under reflux. It was then cooled to room temperature and 20.2 g (0.2 mol) of triethylamine were added dropwise. The mixture was stirred for a further 2 hours at 50° C., the insoluble constituents were filtered off and the filtrate was evaporated in vacuo. The residue was treated with water and the product was filtered off, washed with water and dried. 21.5 g (72.5% of theory) of 2-(4,5-dichloro-imidazol-2-yl)-5-phenoxy-1,3,4-oxadiazole were obtained. Melting point: 109° C. (from toluene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369186
Source datasetuspto-grants-1983_01
ORD IDord-d7276870b2c145e1877af41999adc4fd
Source noteuspto-grants-1983_01