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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381139Generated: October 26, 2026

Triethylamine → 2,4-difluoro-alpha-(1H-1,2,4-triazol-1-yl)acetophenone hydrochloride

https://huagongshe.com/reaction/1381139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant2-Chloro-1-(2,4-difluorophenyl)ethanoneHCID 588083—
SolventEthyl AcetateHCID 8857—
Product2,4-difluoro-alpha-(1H-1,2,4-triazol-1-yl)acetophenone hydrochlorideHCID 1305969941.6%

Reaction Steps

To a mixture of 1,2,4-triazole (30.4 g, 0.44M) and triethylamine (15.1 g, 0.15M) in refluxing ethyl acetate (186 ml) was added a solution of 2-chloro-2',4'-difluoroacetophenone (38.1 g, 0.2M) in ethyl acetate (80 ml). The mixture was refluxed for six hours then cooled to room temperature and the insolubles were removed by filtration. The filtrate was washed with water (2×200 ml) and then the solvent was removed by distillation at reduced pressure. The crude product was dissolved in ethyl acetate (150 ml) then 25% w/v HCl gas in isopropanol was added. The mixture was granulated at 0° C. for one hour and then the solid was collected by filtration and dried to give the title compound (21.6 g, 40%), melting point 167°-170° C. IR (KBr) and nmr (DMSO) were consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585778
Source datasetuspto-grants-1986_04
ORD IDord-5e958b564b884fa9a78e8f5bdac9abc4
Source noteuspto-grants-1986_04