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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydrazinecarboxylic acid, phenyl ester | HCID 134791 | — |
| Reactant | 4,5-Dichloro-2-(trichloromethyl)-1H-imidazole | HCID 12482573 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4,5-Dichloro-imidazol-2-yl)-5-phenoxy-1,3,4-oxadiazole | HCID 135755445 | 72.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04369186 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-d7276870b2c145e1877af41999adc4fd |
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| Source note | uspto-grants-1983_01 |
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